@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:NP1381128.RA_1fhLptJPe7_qfLBBZj0e2DVV1iM5wNHR11kqaDVbag130_head { this: np:hasAssertion dgn-np:NP1381128.RA_1fhLptJPe7_qfLBBZj0e2DVV1iM5wNHR11kqaDVbag130_assertion; np:hasProvenance dgn-np:NP1381128.RA_1fhLptJPe7_qfLBBZj0e2DVV1iM5wNHR11kqaDVbag130_provenance; np:hasPublicationInfo dgn-np:NP1381128.RA_1fhLptJPe7_qfLBBZj0e2DVV1iM5wNHR11kqaDVbag130_publicationInfo; a np:Nanopublication . dgn-np:NP1381128.RA_1fhLptJPe7_qfLBBZj0e2DVV1iM5wNHR11kqaDVbag130_assertion a np:Assertion . dgn-np:NP1381128.RA_1fhLptJPe7_qfLBBZj0e2DVV1iM5wNHR11kqaDVbag130_provenance a np:Provenance . dgn-np:NP1381128.RA_1fhLptJPe7_qfLBBZj0e2DVV1iM5wNHR11kqaDVbag130_publicationInfo a np:PublicationInfo . } dgn-np:NP1381128.RA_1fhLptJPe7_qfLBBZj0e2DVV1iM5wNHR11kqaDVbag130_assertion { miriam-gene:4292 a ncit:C16612 . lld:C1333990 a ncit:C7057 . dgn-gda:DGN88c2e5c19fbca7f4e4266de08df48a2b sio:SIO_000628 miriam-gene:4292, lld:C1333990; a sio:SIO_001121 . } dgn-np:NP1381128.RA_1fhLptJPe7_qfLBBZj0e2DVV1iM5wNHR11kqaDVbag130_provenance { dgn-np:NP1381128.RA_1fhLptJPe7_qfLBBZj0e2DVV1iM5wNHR11kqaDVbag130_assertion dcterms:description "[Here, we applied denaturing gradient-gel electrophoresis to screen for hMSH2 and hMLH1 mutations in two sets of HNPCC families, one set comprising families strictly complying with the Amsterdam criteria and another set in which at least one of the criteria was not satisfied.]. 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:9311737; 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:NP1381128.RA_1fhLptJPe7_qfLBBZj0e2DVV1iM5wNHR11kqaDVbag130_publicationInfo { this: dcterms:created "2016-05-13T12:52:12+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" . }