@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:NP335397.RA6pHw4uZtQCOQ9mdCnln2HUT4aO5f9tvfGJnhmtv8ODE130_head { this: np:hasAssertion dgn-np:NP335397.RA6pHw4uZtQCOQ9mdCnln2HUT4aO5f9tvfGJnhmtv8ODE130_assertion; np:hasProvenance dgn-np:NP335397.RA6pHw4uZtQCOQ9mdCnln2HUT4aO5f9tvfGJnhmtv8ODE130_provenance; np:hasPublicationInfo dgn-np:NP335397.RA6pHw4uZtQCOQ9mdCnln2HUT4aO5f9tvfGJnhmtv8ODE130_publicationInfo; a np:Nanopublication . dgn-np:NP335397.RA6pHw4uZtQCOQ9mdCnln2HUT4aO5f9tvfGJnhmtv8ODE130_assertion a np:Assertion . dgn-np:NP335397.RA6pHw4uZtQCOQ9mdCnln2HUT4aO5f9tvfGJnhmtv8ODE130_provenance a np:Provenance . dgn-np:NP335397.RA6pHw4uZtQCOQ9mdCnln2HUT4aO5f9tvfGJnhmtv8ODE130_publicationInfo a np:PublicationInfo . } dgn-np:NP335397.RA6pHw4uZtQCOQ9mdCnln2HUT4aO5f9tvfGJnhmtv8ODE130_assertion { miriam-gene:64127 a ncit:C16612 . lld:C0021390 a ncit:C7057 . dgn-gda:DGN7cea4f7dea2afd53b36ee2e776ce6bea sio:SIO_000628 miriam-gene:64127, lld:C0021390; a sio:SIO_001121 . } dgn-np:NP335397.RA6pHw4uZtQCOQ9mdCnln2HUT4aO5f9tvfGJnhmtv8ODE130_provenance { dgn-np:NP335397.RA6pHw4uZtQCOQ9mdCnln2HUT4aO5f9tvfGJnhmtv8ODE130_assertion dcterms:description "[Recent studies have established that at least three coding region variants in the Nod2 gene are responsible for the linkage findings here, and Nod2 therefore represents the first definitively established gene contributing to the pathogenesis of IBD.]. 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:11696282; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP335397.RA6pHw4uZtQCOQ9mdCnln2HUT4aO5f9tvfGJnhmtv8ODE130_publicationInfo { this: dcterms:created "2016-05-13T12:44:17+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 "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }