@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:NP421880.RAe0I0Fy_8uT-56phnMCh-W6pwWZy_PX8NkBm7WcBPEBY130_head { this: np:hasAssertion dgn-np:NP421880.RAe0I0Fy_8uT-56phnMCh-W6pwWZy_PX8NkBm7WcBPEBY130_assertion; np:hasProvenance dgn-np:NP421880.RAe0I0Fy_8uT-56phnMCh-W6pwWZy_PX8NkBm7WcBPEBY130_provenance; np:hasPublicationInfo dgn-np:NP421880.RAe0I0Fy_8uT-56phnMCh-W6pwWZy_PX8NkBm7WcBPEBY130_publicationInfo; a np:Nanopublication . dgn-np:NP421880.RAe0I0Fy_8uT-56phnMCh-W6pwWZy_PX8NkBm7WcBPEBY130_assertion a np:Assertion . dgn-np:NP421880.RAe0I0Fy_8uT-56phnMCh-W6pwWZy_PX8NkBm7WcBPEBY130_provenance a np:Provenance . dgn-np:NP421880.RAe0I0Fy_8uT-56phnMCh-W6pwWZy_PX8NkBm7WcBPEBY130_publicationInfo a np:PublicationInfo . } dgn-np:NP421880.RAe0I0Fy_8uT-56phnMCh-W6pwWZy_PX8NkBm7WcBPEBY130_assertion { miriam-gene:2651 a ncit:C16612 . lld:C1527249 a ncit:C7057 . dgn-gda:DGN765c2cc374b6cf87644b4678e36ddd2d sio:SIO_000628 miriam-gene:2651, lld:C1527249; a sio:SIO_001122 . } dgn-np:NP421880.RAe0I0Fy_8uT-56phnMCh-W6pwWZy_PX8NkBm7WcBPEBY130_provenance { dgn-np:NP421880.RAe0I0Fy_8uT-56phnMCh-W6pwWZy_PX8NkBm7WcBPEBY130_assertion dcterms:description "[We analyzed microsatellite instability, alterations of the polyadenine tract in TGF-beta RII (transforming growth factor beta type II receptor gene), and mutations of hMSH2 and hMLH1 in 32 patients with familial colorectal cancer (29 kindreds) fulfilling the clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC), defined at the 34th Annual Meeting of Japanese Society for Cancer of the Colon and Rectum (Tokushima, Japan, 1991), including five kindreds fulfilling the Amsterdam criteria.]. 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:9419403; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP421880.RAe0I0Fy_8uT-56phnMCh-W6pwWZy_PX8NkBm7WcBPEBY130_publicationInfo { this: dcterms:created "2015-08-25T14:41:45+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }