@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:NP1053679.RAVJ4wyaARJk46Ob8d_n7aVkXnRGaFYMvliMr64zPSRaw130_head { this: np:hasAssertion dgn-np:NP1053679.RAVJ4wyaARJk46Ob8d_n7aVkXnRGaFYMvliMr64zPSRaw130_assertion; np:hasProvenance dgn-np:NP1053679.RAVJ4wyaARJk46Ob8d_n7aVkXnRGaFYMvliMr64zPSRaw130_provenance; np:hasPublicationInfo dgn-np:NP1053679.RAVJ4wyaARJk46Ob8d_n7aVkXnRGaFYMvliMr64zPSRaw130_publicationInfo; a np:Nanopublication . dgn-np:NP1053679.RAVJ4wyaARJk46Ob8d_n7aVkXnRGaFYMvliMr64zPSRaw130_assertion a np:Assertion . dgn-np:NP1053679.RAVJ4wyaARJk46Ob8d_n7aVkXnRGaFYMvliMr64zPSRaw130_provenance a np:Provenance . dgn-np:NP1053679.RAVJ4wyaARJk46Ob8d_n7aVkXnRGaFYMvliMr64zPSRaw130_publicationInfo a np:PublicationInfo . } dgn-np:NP1053679.RAVJ4wyaARJk46Ob8d_n7aVkXnRGaFYMvliMr64zPSRaw130_assertion { miriam-gene:4436 a ncit:C16612 . lld:C1333990 a ncit:C7057 . dgn-gda:DGNf7d17bcc810500bc4688ea4fe6c1ca9a sio:SIO_000628 miriam-gene:4436, lld:C1333990; a sio:SIO_001121 . } dgn-np:NP1053679.RAVJ4wyaARJk46Ob8d_n7aVkXnRGaFYMvliMr64zPSRaw130_provenance { dgn-np:NP1053679.RAVJ4wyaARJk46Ob8d_n7aVkXnRGaFYMvliMr64zPSRaw130_assertion dcterms:description "[The associated familial cancer susceptibility syndromes are familial adenomatous polyposis coli, due to inherited APC mutations, and Lynch Syndrome or hereditary nonpolyposis colorectal cancer syndrome, due to inherited mutations in one of the mismatch repair genes (predominantly MLH1 and MSH2).]. 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:23417071; 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:NP1053679.RAVJ4wyaARJk46Ob8d_n7aVkXnRGaFYMvliMr64zPSRaw130_publicationInfo { this: dcterms:created "2016-05-13T12:49:44+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" . }