@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:NP1116973.RAqEmxEc5aJ5Cc99FCCip-cCnwhN9WwgXrefcVF-QI6x8130_head { this: np:hasAssertion dgn-np:NP1116973.RAqEmxEc5aJ5Cc99FCCip-cCnwhN9WwgXrefcVF-QI6x8130_assertion; np:hasProvenance dgn-np:NP1116973.RAqEmxEc5aJ5Cc99FCCip-cCnwhN9WwgXrefcVF-QI6x8130_provenance; np:hasPublicationInfo dgn-np:NP1116973.RAqEmxEc5aJ5Cc99FCCip-cCnwhN9WwgXrefcVF-QI6x8130_publicationInfo; a np:Nanopublication . dgn-np:NP1116973.RAqEmxEc5aJ5Cc99FCCip-cCnwhN9WwgXrefcVF-QI6x8130_assertion a np:Assertion . dgn-np:NP1116973.RAqEmxEc5aJ5Cc99FCCip-cCnwhN9WwgXrefcVF-QI6x8130_provenance a np:Provenance . dgn-np:NP1116973.RAqEmxEc5aJ5Cc99FCCip-cCnwhN9WwgXrefcVF-QI6x8130_publicationInfo a np:PublicationInfo . } dgn-np:NP1116973.RAqEmxEc5aJ5Cc99FCCip-cCnwhN9WwgXrefcVF-QI6x8130_assertion { miriam-gene:4292 a ncit:C16612 . lld:C0009404 a ncit:C7057 . dgn-gda:DGN053eeba58163ebf015deb8370db0bcad sio:SIO_000628 miriam-gene:4292, lld:C0009404; a sio:SIO_001121 . } dgn-np:NP1116973.RAqEmxEc5aJ5Cc99FCCip-cCnwhN9WwgXrefcVF-QI6x8130_provenance { dgn-np:NP1116973.RAqEmxEc5aJ5Cc99FCCip-cCnwhN9WwgXrefcVF-QI6x8130_assertion dcterms:description "[We investigated the clinical and molecular features of the MSH6 variants, such as the family cancer history, pathological findings, immunohistochemistry, methylation status of the MLH1 promoter and BRAF mutation in the colorectal tumor.]. 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:24100870; 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:NP1116973.RAqEmxEc5aJ5Cc99FCCip-cCnwhN9WwgXrefcVF-QI6x8130_publicationInfo { this: dcterms:created "2016-05-13T12:50:12+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" . }