@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:NP979076.RApAuSPTym6_W9M7BJp9v3dqdhHHtF2R7PlfiWaiPBnnY130_head { this: np:hasAssertion dgn-np:NP979076.RApAuSPTym6_W9M7BJp9v3dqdhHHtF2R7PlfiWaiPBnnY130_assertion; np:hasProvenance dgn-np:NP979076.RApAuSPTym6_W9M7BJp9v3dqdhHHtF2R7PlfiWaiPBnnY130_provenance; np:hasPublicationInfo dgn-np:NP979076.RApAuSPTym6_W9M7BJp9v3dqdhHHtF2R7PlfiWaiPBnnY130_publicationInfo; a np:Nanopublication . dgn-np:NP979076.RApAuSPTym6_W9M7BJp9v3dqdhHHtF2R7PlfiWaiPBnnY130_assertion a np:Assertion . dgn-np:NP979076.RApAuSPTym6_W9M7BJp9v3dqdhHHtF2R7PlfiWaiPBnnY130_provenance a np:Provenance . dgn-np:NP979076.RApAuSPTym6_W9M7BJp9v3dqdhHHtF2R7PlfiWaiPBnnY130_publicationInfo a np:PublicationInfo . } dgn-np:NP979076.RApAuSPTym6_W9M7BJp9v3dqdhHHtF2R7PlfiWaiPBnnY130_assertion { miriam-gene:4072 a ncit:C16612 . lld:C1333990 a ncit:C7057 . dgn-gda:DGNf1215e85ccecbf3cbe613e159a72f383 sio:SIO_000628 miriam-gene:4072, lld:C1333990; a sio:SIO_001121 . } dgn-np:NP979076.RApAuSPTym6_W9M7BJp9v3dqdhHHtF2R7PlfiWaiPBnnY130_provenance { dgn-np:NP979076.RApAuSPTym6_W9M7BJp9v3dqdhHHtF2R7PlfiWaiPBnnY130_assertion dcterms:description "[We systematically analysed non-tumorous mucosa from carriers of a Lynch syndrome mutation (set 1: ten patients) and control patients without Lynch syndrome (set 1: nine patients) for MMR protein expression (MLH1, MSH2, and EPCAM) with immunohistochemistry.]. 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:22552011; 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:NP979076.RApAuSPTym6_W9M7BJp9v3dqdhHHtF2R7PlfiWaiPBnnY130_publicationInfo { this: dcterms:created "2016-05-13T12:49:08+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" . }