@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP119595.RAdSgF7aNx30o8DUZsF2P3wt_Dj2dcguc9D8LpJOhCInM130_head { this: np:hasAssertion dgn-np:NP119595.RAdSgF7aNx30o8DUZsF2P3wt_Dj2dcguc9D8LpJOhCInM130_assertion; np:hasProvenance dgn-np:NP119595.RAdSgF7aNx30o8DUZsF2P3wt_Dj2dcguc9D8LpJOhCInM130_provenance; np:hasPublicationInfo dgn-np:NP119595.RAdSgF7aNx30o8DUZsF2P3wt_Dj2dcguc9D8LpJOhCInM130_publicationInfo; a np:Nanopublication . dgn-np:NP119595.RAdSgF7aNx30o8DUZsF2P3wt_Dj2dcguc9D8LpJOhCInM130_assertion a np:Assertion . dgn-np:NP119595.RAdSgF7aNx30o8DUZsF2P3wt_Dj2dcguc9D8LpJOhCInM130_provenance a np:Provenance . dgn-np:NP119595.RAdSgF7aNx30o8DUZsF2P3wt_Dj2dcguc9D8LpJOhCInM130_publicationInfo a np:PublicationInfo . } dgn-np:NP119595.RAdSgF7aNx30o8DUZsF2P3wt_Dj2dcguc9D8LpJOhCInM130_assertion { miriam-gene:7473 a ncit:C16612 . lld:C0008924 a ncit:C7057 . dgn-gda:DGN51ed4cd99cafc1c38727cb75b65915bb sio:SIO_000628 miriam-gene:7473, lld:C0008924; a sio:SIO_001122 . } dgn-np:NP119595.RAdSgF7aNx30o8DUZsF2P3wt_Dj2dcguc9D8LpJOhCInM130_provenance { dgn-np:NP119595.RAdSgF7aNx30o8DUZsF2P3wt_Dj2dcguc9D8LpJOhCInM130_assertion dcterms:description "[This study provides for the first time evidence of the implication of IRF6, COL2A1, and WNT3 in the occurrence of NSCP. It is likely that variation in cartilage collagen II and XI genes, IRF6, and the Wnt and FGF signaling pathway genes contributes suscep]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:20672350; prov:wasDerivedFrom dgn-void:gad-20150221; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP119595.RAdSgF7aNx30o8DUZsF2P3wt_Dj2dcguc9D8LpJOhCInM130_publicationInfo { this: dcterms:created "2015-08-25T14:38:47+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }