@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:NP423088.RAqMnJbSethdgfi_R8eHdGs3UFOwdrMFjaQakx3IocLdw130_head { this: np:hasAssertion dgn-np:NP423088.RAqMnJbSethdgfi_R8eHdGs3UFOwdrMFjaQakx3IocLdw130_assertion; np:hasProvenance dgn-np:NP423088.RAqMnJbSethdgfi_R8eHdGs3UFOwdrMFjaQakx3IocLdw130_provenance; np:hasPublicationInfo dgn-np:NP423088.RAqMnJbSethdgfi_R8eHdGs3UFOwdrMFjaQakx3IocLdw130_publicationInfo; a np:Nanopublication . dgn-np:NP423088.RAqMnJbSethdgfi_R8eHdGs3UFOwdrMFjaQakx3IocLdw130_assertion a np:Assertion . dgn-np:NP423088.RAqMnJbSethdgfi_R8eHdGs3UFOwdrMFjaQakx3IocLdw130_provenance a np:Provenance . dgn-np:NP423088.RAqMnJbSethdgfi_R8eHdGs3UFOwdrMFjaQakx3IocLdw130_publicationInfo a np:PublicationInfo . } dgn-np:NP423088.RAqMnJbSethdgfi_R8eHdGs3UFOwdrMFjaQakx3IocLdw130_assertion { miriam-gene:4360 a ncit:C16612 . lld:C1333990 a ncit:C7057 . dgn-gda:DGNb19f6cc34505b081a4f276bb7819a7aa sio:SIO_000628 miriam-gene:4360, lld:C1333990; a sio:SIO_001121 . } dgn-np:NP423088.RAqMnJbSethdgfi_R8eHdGs3UFOwdrMFjaQakx3IocLdw130_provenance { dgn-np:NP423088.RAqMnJbSethdgfi_R8eHdGs3UFOwdrMFjaQakx3IocLdw130_assertion dcterms:description "[MMR protein immunostaining facilitates mutation analysis in suspected HNPCC patients, since it pinpoints the mutated gene, but until the genetic background to the MSI tumors with retained MMR protein expression has been clarified, we suggest that MSI and MMR protein immunostaining should optimally be combined in clinical HNPCC analysis.]. 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:14652751; 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:NP423088.RAqMnJbSethdgfi_R8eHdGs3UFOwdrMFjaQakx3IocLdw130_publicationInfo { this: dcterms:created "2016-05-13T12:44:57+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" . }