提供：TogoWiki
ensembl_variant:rs766173 dc:identifier "rs766173" .
ensembl_variant:rs766173 rdfs:label "rs766173" .
- Class:SO_0001483: SNV (subclass of sequence_alteration)
ensembl_variant:rs766173 a obo:SO_0001483 .
- 目的語はOriginal sourceから？
- DatatypeProperty:has_source: Source information for either data imported into Ensembl Variation or for phenotype associations.
ensembl_variant:rs766173 ensemblvariation:has_source "dbSNP" .
ensembl_variant:rs766173 skos:altLabel "NM_000059.3:c.865A>G" .
ensembl_variant:rs766173 skos:altLabel "NM_000059.3:c.865A>C" .
ensembl_variant:rs766173 skos:altLabel "rs52810428" .
ensembl_variant:rs766173 skos:altLabel "rs1801384" .
ensembl_variant:rs766173 skos:altLabel "VAR_005092" .
- Clinical significanceから
- has_clinical_significance は ObjectProperty だが、目的語がなぜかリテラル
- ensembl_variation_ontology.owl には clinical_significance というクラスも存在
ensembl_variant:rs766173 ensemblvariation:has_clinical_significance "uncertain significance" .
ensembl_variant:rs766173 ensemblvariation:has_clinical_significance "not provided" .
ensembl_variant:rs766173 ensemblvariation:has_clinical_significance "benign" .
- どこから？
- has_phenotype_annotation: OWLファイル・スキーマに記述なし
ensembl_variant:rs766173 ensemblvariation:has_phenotype_annotation "Neoplastic Syndromes, Hereditary" .
ensembl_variant:rs766173 ensemblvariation:has_phenotype_annotation "AllHighlyPenetrant" .
ensembl_variant:rs766173 ensemblvariation:has_phenotype_annotation "Breast-ovarian cancer, familial 2" .
ensembl_variant:rs766173 ensemblvariation:has_phenotype_annotation "Familial cancer of breast" .
ensembl_variant:rs766173 ensemblvariation:has_phenotype_annotation "Breast-ovarian cancer, familial 2" .
- FALDOによる位置情報
- Locationから
- begin-endが同じなのでExactPositionは一組でいいはず（バグ？）ただし、INDEL等でbegin-endが異なることはあり得る
ensembl_variant:rs766173 faldo:location <http://rdf.ebi.ac.uk/resource/ensembl/77/chromosome:GRCh38:13:32332343-32332343:1> .
<http://rdf.ebi.ac.uk/resource/ensembl/77/chromosome:GRCh38:13:32332343-32332343:1> rdfs:label "chromosome 13:32332343-32332343:1" .
<http://rdf.ebi.ac.uk/resource/ensembl/77/chromosome:GRCh38:13:32332343-32332343:1> rdf:type faldo:Region .
<http://rdf.ebi.ac.uk/resource/ensembl/77/chromosome:GRCh38:13:32332343-32332343:1> faldo:begin <http://rdf.ebi.ac.uk/resource/ensembl/77/chromosome:GRCh38:13:32332343:1> .
<http://rdf.ebi.ac.uk/resource/ensembl/77/chromosome:GRCh38:13:32332343-32332343:1> faldo:end <http://rdf.ebi.ac.uk/resource/ensembl/77/chromosome:GRCh38:13:32332343:1> .
<http://rdf.ebi.ac.uk/resource/ensembl/77/chromosome:GRCh38:13:32332343-32332343:1> faldo:reference <http://rdf.ebi.ac.uk/resource/ensembl/77/chromosome:GRCh38:13> .
<http://rdf.ebi.ac.uk/resource/ensembl/77/chromosome:GRCh38:13:32332343:1> rdf:type faldo:ExactPosition .
<http://rdf.ebi.ac.uk/resource/ensembl/77/chromosome:GRCh38:13:32332343:1> rdf:type faldo:ForwardStrandPosition .
<http://rdf.ebi.ac.uk/resource/ensembl/77/chromosome:GRCh38:13:32332343:1> faldo:position 32332343 .
<http://rdf.ebi.ac.uk/resource/ensembl/77/chromosome:GRCh38:13:32332343:1> faldo:reference <http://rdf.ebi.ac.uk/resource/ensembl/77/chromosome:GRCh38:13> .
<http://rdf.ebi.ac.uk/resource/ensembl/77/chromosome:GRCh38:13:32332343:1> rdf:type faldo:ExactPosition .
<http://rdf.ebi.ac.uk/resource/ensembl/77/chromosome:GRCh38:13:32332343:1> rdf:type faldo:ForwardStrandPosition .
<http://rdf.ebi.ac.uk/resource/ensembl/77/chromosome:GRCh38:13:32332343:1> faldo:position 32332343 .
<http://rdf.ebi.ac.uk/resource/ensembl/77/chromosome:GRCh38:13:32332343:1> faldo:reference <http://rdf.ebi.ac.uk/resource/ensembl/77/chromosome:GRCh38:13> .
- Allelesから
- ObjectProperty:has_allele
- Class:reference_allele: Allele as defined against a reference genome build.
- Class:ancestral_allele: The allele that was carried by the common ancestor of the taxon you consider.
- Class:minor_allele: Least frequently observed allele in a given data set.
- Class:derived_allele: An allele which is not defined as the ancestral allele.
- メジャーアレル？の型定義（derived_allele?）がない
ensembl_variant:rs766173 ensemblvariation:has_allele ensembl_variant:rs766173#A .
ensembl_variant:rs766173#A rdfs:label "rs766173 allele A" .
ensembl_variant:rs766173#A a ensemblvariation:reference_allele .
ensembl_variant:rs766173#A a ensemblvariation:ancestral_allele .
ensembl_variant:rs766173 ensemblvariation:has_allele ensembl_variant:rs766173#C .
ensembl_variant:rs766173#C rdfs:label "rs766173 allele C" .
ensembl_variant:rs766173#C a ensemblvariation:minor_allele .
ensembl_variant:rs766173 ensemblvariation:has_allele ensembl_variant:rs766173#G .
ensembl_variant:rs766173#G rdfs:label "rs766173 allele G" .
- Most severe consequenceのリンク先から
- ObjectProperty:has_variant_effect
ensembl_variant:rs766173#C ensemblvariation:has_variant_effect ensembl_variant:ENST00000544455_rs766173#C .
- Transcriptから
- so_overlaps: X overlaps Y iff there exists some Z such that Z contained_by X and Z contained_by Y.
ensembl_variant:ENST00000544455_rs766173#C obo:so_overlaps transcript:ENST00000544455 .
- Class:SO_0001583: missense_variant (subClass of gene_variant)
ensembl_variant:ENST00000544455_rs766173#C a obo:SO_0001583 .
- Showを押すと出てくる HGVS names から
- DatatypeProperty:has_HGVS_transcript_name (subClass of has_HGVS_name)
- DatatypeProperty:has_HGVS_protein_name (subClass of has_HGVS_name)
- ウェブページではTranscriptとProteinは区別されていないが、RDFでは区別している
ensembl_variant:ENST00000544455_rs766173#C ensemblvariation:has_HGVS_transcript_name "ENST00000544455.3:c.865A>C" .
ensembl_variant:ENST00000544455_rs766173#C ensemblvariation:has_HGVS_protein_name "ENSP00000439902.1:p.Asn289His" .
- SIFT/PolyPhenから
- ブランクノードをはさんだほうが良いのでは？
- OWLにはhas_SIFT_score/has_PolyPhen_scoreがあるのでバグっぽい
ensembl_variant:ENST00000544455_rs766173#C ensemblvariation:has_SIFT_prediction "tolerated" .
ensembl_variant:ENST00000544455_rs766173#C ensemblvariation:has_SIFT_prediction "0.06"^^xsd:float .
ensembl_variant:ENST00000544455_rs766173#C ensemblvariation:has_PolyPhen_prediction "benign" .
ensembl_variant:ENST00000544455_rs766173#C ensemblvariation:has_PolyPhen_prediction "0.052"^^xsd:float .
ensembl_variant:ENST00000544455_rs766173#C ensemblvariation:has_reference_peptide_sequence "N" .
ensembl_variant:ENST00000544455_rs766173#C ensemblvariation:has_alternate_peptide_sequence "H" .
ensembl_variant:rs766173#G ensemblvariation:has_variant_effect ensembl_variant:ENST00000544455_rs766173#G .
ensembl_variant:ENST00000544455_rs766173#G obo:so_overlaps transcript:ENST00000544455 .
ensembl_variant:ENST00000544455_rs766173#G a obo:SO_0001583 .
ensembl_variant:ENST00000544455_rs766173#G ensemblvariation:has_HGVS_transcript_name "ENST00000544455.3:c.865A>G" .
ensembl_variant:ENST00000544455_rs766173#G ensemblvariation:has_HGVS_protein_name "ENSP00000439902.1:p.Asn289Asp" .
ensembl_variant:ENST00000544455_rs766173#G ensemblvariation:has_SIFT_prediction "tolerated" .
ensembl_variant:ENST00000544455_rs766173#G ensemblvariation:has_SIFT_prediction "0.07"^^xsd:float .
ensembl_variant:ENST00000544455_rs766173#G ensemblvariation:has_PolyPhen_prediction "benign" .
ensembl_variant:ENST00000544455_rs766173#G ensemblvariation:has_PolyPhen_prediction "0.022"^^xsd:float .
ensembl_variant:ENST00000544455_rs766173#G ensemblvariation:has_reference_peptide_sequence "N" .
ensembl_variant:ENST00000544455_rs766173#G ensemblvariation:has_alternate_peptide_sequence "D" .
ensembl_variant:rs766173#C ensemblvariation:has_variant_effect ensembl_variant:LRG_293t1_rs766173#C .
ensembl_variant:LRG_293t1_rs766173#C obo:so_overlaps transcript:LRG_293t1 .
ensembl_variant:LRG_293t1_rs766173#C a obo:SO_0001583 .
ensembl_variant:LRG_293t1_rs766173#C ensemblvariation:has_HGVS_transcript_name "LRG_293t1.1:c.865A>C" .
ensembl_variant:LRG_293t1_rs766173#C ensemblvariation:has_HGVS_protein_name "LRG_293p1.1:p.Asn289His" .
ensembl_variant:LRG_293t1_rs766173#C ensemblvariation:has_SIFT_prediction "tolerated" .
ensembl_variant:LRG_293t1_rs766173#C ensemblvariation:has_SIFT_prediction "0.06"^^xsd:float .
ensembl_variant:LRG_293t1_rs766173#C ensemblvariation:has_PolyPhen_prediction "benign" .
ensembl_variant:LRG_293t1_rs766173#C ensemblvariation:has_PolyPhen_prediction "0.052"^^xsd:float .
ensembl_variant:LRG_293t1_rs766173#C ensemblvariation:has_reference_peptide_sequence "N" .
ensembl_variant:LRG_293t1_rs766173#C ensemblvariation:has_alternate_peptide_sequence "H" .
ensembl_variant:rs766173#G ensemblvariation:has_variant_effect ensembl_variant:LRG_293t1_rs766173#G .
ensembl_variant:LRG_293t1_rs766173#G obo:so_overlaps transcript:LRG_293t1 .
ensembl_variant:LRG_293t1_rs766173#G a obo:SO_0001583 .
ensembl_variant:LRG_293t1_rs766173#G ensemblvariation:has_HGVS_transcript_name "LRG_293t1.1:c.865A>G" .
ensembl_variant:LRG_293t1_rs766173#G ensemblvariation:has_HGVS_protein_name "LRG_293p1.1:p.Asn289Asp" .
ensembl_variant:LRG_293t1_rs766173#G ensemblvariation:has_SIFT_prediction "tolerated" .
ensembl_variant:LRG_293t1_rs766173#G ensemblvariation:has_SIFT_prediction "0.07"^^xsd:float .
ensembl_variant:LRG_293t1_rs766173#G ensemblvariation:has_PolyPhen_prediction "benign" .
ensembl_variant:LRG_293t1_rs766173#G ensemblvariation:has_PolyPhen_prediction "0.022"^^xsd:float .
ensembl_variant:LRG_293t1_rs766173#G ensemblvariation:has_reference_peptide_sequence "N" .
ensembl_variant:LRG_293t1_rs766173#G ensemblvariation:has_alternate_peptide_sequence "D" .
ensembl_variant:rs766173#C ensemblvariation:has_variant_effect ensembl_variant:ENST00000530893_rs766173#C .
ensembl_variant:ENST00000530893_rs766173#C obo:so_overlaps transcript:ENST00000530893 .
ensembl_variant:ENST00000530893_rs766173#C a obo:SO_0001619 .
ensembl_variant:ENST00000530893_rs766173#C a obo:SO_0001792 .
ensembl_variant:ENST00000530893_rs766173#C ensemblvariation:has_HGVS_transcript_name "ENST00000530893.4:n.1063A>C" .
ensembl_variant:rs766173#G ensemblvariation:has_variant_effect ensembl_variant:ENST00000530893_rs766173#G .
ensembl_variant:ENST00000530893_rs766173#G obo:so_overlaps transcript:ENST00000530893 .
ensembl_variant:ENST00000530893_rs766173#G a obo:SO_0001619 .
ensembl_variant:ENST00000530893_rs766173#G a obo:SO_0001792 .
ensembl_variant:ENST00000530893_rs766173#G ensemblvariation:has_HGVS_transcript_name "ENST00000530893.4:n.1063A>G" .
ensembl_variant:rs766173#C ensemblvariation:has_variant_effect ensembl_variant:ENST00000380152_rs766173#C .
ensembl_variant:ENST00000380152_rs766173#C obo:so_overlaps transcript:ENST00000380152 .
ensembl_variant:ENST00000380152_rs766173#C a obo:SO_0001583 .
ensembl_variant:ENST00000380152_rs766173#C ensemblvariation:has_HGVS_transcript_name "ENST00000380152.5:c.865A>C" .
ensembl_variant:ENST00000380152_rs766173#C ensemblvariation:has_HGVS_protein_name "ENSP00000369497.3:p.Asn289His" .
ensembl_variant:ENST00000380152_rs766173#C ensemblvariation:has_SIFT_prediction "tolerated" .
ensembl_variant:ENST00000380152_rs766173#C ensemblvariation:has_SIFT_prediction "0.06"^^xsd:float .
ensembl_variant:ENST00000380152_rs766173#C ensemblvariation:has_PolyPhen_prediction "benign" .
ensembl_variant:ENST00000380152_rs766173#C ensemblvariation:has_PolyPhen_prediction "0.052"^^xsd:float .
ensembl_variant:ENST00000380152_rs766173#C ensemblvariation:has_reference_peptide_sequence "N" .
ensembl_variant:ENST00000380152_rs766173#C ensemblvariation:has_alternate_peptide_sequence "H" .
ensembl_variant:rs766173#G ensemblvariation:has_variant_effect ensembl_variant:ENST00000380152_rs766173#G .
ensembl_variant:ENST00000380152_rs766173#G obo:so_overlaps transcript:ENST00000380152 .
ensembl_variant:ENST00000380152_rs766173#G a obo:SO_0001583 .
ensembl_variant:ENST00000380152_rs766173#G ensemblvariation:has_HGVS_transcript_name "ENST00000380152.5:c.865A>G" .
ensembl_variant:ENST00000380152_rs766173#G ensemblvariation:has_HGVS_protein_name "ENSP00000369497.3:p.Asn289Asp" .
ensembl_variant:ENST00000380152_rs766173#G ensemblvariation:has_SIFT_prediction "tolerated" .
ensembl_variant:ENST00000380152_rs766173#G ensemblvariation:has_SIFT_prediction "0.07"^^xsd:float .
ensembl_variant:ENST00000380152_rs766173#G ensemblvariation:has_PolyPhen_prediction "benign" .
ensembl_variant:ENST00000380152_rs766173#G ensemblvariation:has_PolyPhen_prediction "0.022"^^xsd:float .
ensembl_variant:ENST00000380152_rs766173#G ensemblvariation:has_reference_peptide_sequence "N" .
ensembl_variant:ENST00000380152_rs766173#G ensemblvariation:has_alternate_peptide_sequence "D" .
ensembl_variant:rs766173#C ensemblvariation:has_variant_effect ensembl_variant:ENST00000614259_rs766173#C .
ensembl_variant:ENST00000614259_rs766173#C obo:so_overlaps transcript:ENST00000614259 .
ensembl_variant:ENST00000614259_rs766173#C a obo:SO_0001619 .
ensembl_variant:ENST00000614259_rs766173#C a obo:SO_0001792 .
ensembl_variant:ENST00000614259_rs766173#C ensemblvariation:has_HGVS_transcript_name "ENST00000614259.1:n.865A>C" .
ensembl_variant:rs766173#G ensemblvariation:has_variant_effect ensembl_variant:ENST00000614259_rs766173#G .
ensembl_variant:ENST00000614259_rs766173#G obo:so_overlaps transcript:ENST00000614259 .
ensembl_variant:ENST00000614259_rs766173#G a obo:SO_0001619 .
ensembl_variant:ENST00000614259_rs766173#G a obo:SO_0001792 .
ensembl_variant:ENST00000614259_rs766173#G ensemblvariation:has_HGVS_transcript_name "ENST00000614259.1:n.865A>G" .
