@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:NP829111.RAOwz59cWPDTmF5BFVlSDTk6TIICGFwL2nZlkYgzdsvbY130_head { this: np:hasAssertion dgn-np:NP829111.RAOwz59cWPDTmF5BFVlSDTk6TIICGFwL2nZlkYgzdsvbY130_assertion; np:hasProvenance dgn-np:NP829111.RAOwz59cWPDTmF5BFVlSDTk6TIICGFwL2nZlkYgzdsvbY130_provenance; np:hasPublicationInfo dgn-np:NP829111.RAOwz59cWPDTmF5BFVlSDTk6TIICGFwL2nZlkYgzdsvbY130_publicationInfo; a np:Nanopublication . dgn-np:NP829111.RAOwz59cWPDTmF5BFVlSDTk6TIICGFwL2nZlkYgzdsvbY130_assertion a np:Assertion . dgn-np:NP829111.RAOwz59cWPDTmF5BFVlSDTk6TIICGFwL2nZlkYgzdsvbY130_provenance a np:Provenance . dgn-np:NP829111.RAOwz59cWPDTmF5BFVlSDTk6TIICGFwL2nZlkYgzdsvbY130_publicationInfo a np:PublicationInfo . } dgn-np:NP829111.RAOwz59cWPDTmF5BFVlSDTk6TIICGFwL2nZlkYgzdsvbY130_assertion { miriam-gene:4360 a ncit:C16612 . lld:C1333990 a ncit:C7057 . dgn-gda:DGN49a0bde5d5be771b28f09f1fad5a7532 sio:SIO_000628 miriam-gene:4360, lld:C1333990; a sio:SIO_001121 . } dgn-np:NP829111.RAOwz59cWPDTmF5BFVlSDTk6TIICGFwL2nZlkYgzdsvbY130_provenance { dgn-np:NP829111.RAOwz59cWPDTmF5BFVlSDTk6TIICGFwL2nZlkYgzdsvbY130_assertion dcterms:description "[The prevalence of MSI CRC among Hispanic individuals may be similar to that of other races and ethnicities, but clinicopathological characteristics, including age at diagnosis and pattern of abnormal MMR protein expression, suggest that sporadic MSI CRC may be less common in individuals of Hispanic origin, and that much of the MSI observed in this situation may be attributable to Lynch syndrome.]. 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:20665498; 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:NP829111.RAOwz59cWPDTmF5BFVlSDTk6TIICGFwL2nZlkYgzdsvbY130_publicationInfo { this: dcterms:created "2016-05-13T12:48:00+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" . }