@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:NP483999.RAcE4mZ8i9iYRaZxKNUQIgZx14QApqT93n_re1jra4xrM130_head { this: np:hasAssertion dgn-np:NP483999.RAcE4mZ8i9iYRaZxKNUQIgZx14QApqT93n_re1jra4xrM130_assertion; np:hasProvenance dgn-np:NP483999.RAcE4mZ8i9iYRaZxKNUQIgZx14QApqT93n_re1jra4xrM130_provenance; np:hasPublicationInfo dgn-np:NP483999.RAcE4mZ8i9iYRaZxKNUQIgZx14QApqT93n_re1jra4xrM130_publicationInfo; a np:Nanopublication . dgn-np:NP483999.RAcE4mZ8i9iYRaZxKNUQIgZx14QApqT93n_re1jra4xrM130_assertion a np:Assertion . dgn-np:NP483999.RAcE4mZ8i9iYRaZxKNUQIgZx14QApqT93n_re1jra4xrM130_provenance a np:Provenance . dgn-np:NP483999.RAcE4mZ8i9iYRaZxKNUQIgZx14QApqT93n_re1jra4xrM130_publicationInfo a np:PublicationInfo . } dgn-np:NP483999.RAcE4mZ8i9iYRaZxKNUQIgZx14QApqT93n_re1jra4xrM130_assertion { miriam-gene:4360 a ncit:C16612 . lld:C0009402 a ncit:C7057 . dgn-gda:DGNafde4cedb96db35e7283bff3a71a84a2 sio:SIO_000628 miriam-gene:4360, lld:C0009402; a sio:SIO_001121 . } dgn-np:NP483999.RAcE4mZ8i9iYRaZxKNUQIgZx14QApqT93n_re1jra4xrM130_provenance { dgn-np:NP483999.RAcE4mZ8i9iYRaZxKNUQIgZx14QApqT93n_re1jra4xrM130_assertion dcterms:description "[The combination of MSI testing and IHC for MMR proteins in tumors tissues is used to identify underlying DNA MMR deficiency andis clinically relevant screen patients who might have hereditary non-polyposis colorectal cancer for DNA repair gene germline testing.]. 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:15749237; 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:NP483999.RAcE4mZ8i9iYRaZxKNUQIgZx14QApqT93n_re1jra4xrM130_publicationInfo { this: dcterms:created "2016-05-13T12:45:24+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" . }