@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:NP1017841.RAc8DyIoSCWkA-zfg9zA3s8ZJLsOFi1sMfAPDsKkvVhWk130_head { this: np:hasAssertion dgn-np:NP1017841.RAc8DyIoSCWkA-zfg9zA3s8ZJLsOFi1sMfAPDsKkvVhWk130_assertion; np:hasProvenance dgn-np:NP1017841.RAc8DyIoSCWkA-zfg9zA3s8ZJLsOFi1sMfAPDsKkvVhWk130_provenance; np:hasPublicationInfo dgn-np:NP1017841.RAc8DyIoSCWkA-zfg9zA3s8ZJLsOFi1sMfAPDsKkvVhWk130_publicationInfo; a np:Nanopublication . dgn-np:NP1017841.RAc8DyIoSCWkA-zfg9zA3s8ZJLsOFi1sMfAPDsKkvVhWk130_assertion a np:Assertion . dgn-np:NP1017841.RAc8DyIoSCWkA-zfg9zA3s8ZJLsOFi1sMfAPDsKkvVhWk130_provenance a np:Provenance . dgn-np:NP1017841.RAc8DyIoSCWkA-zfg9zA3s8ZJLsOFi1sMfAPDsKkvVhWk130_publicationInfo a np:PublicationInfo . } dgn-np:NP1017841.RAc8DyIoSCWkA-zfg9zA3s8ZJLsOFi1sMfAPDsKkvVhWk130_assertion { miriam-gene:101929889 a ncit:C16612 . lld:C0006826 a ncit:C7057 . dgn-gda:DGN6e1f448d1dd9d994586f45c09e828f89 sio:SIO_000628 miriam-gene:101929889, lld:C0006826; a sio:SIO_001121 . } dgn-np:NP1017841.RAc8DyIoSCWkA-zfg9zA3s8ZJLsOFi1sMfAPDsKkvVhWk130_provenance { dgn-np:NP1017841.RAc8DyIoSCWkA-zfg9zA3s8ZJLsOFi1sMfAPDsKkvVhWk130_assertion dcterms:description "[This is the first report of genetic alterations in the spn gene in a human malignancy and suggests that genetic alterations in spn and the resulting immunohistochemical phenotypes based on SPN subcellular localization in CRCs may be useful in determining prognosis of patients with subtypes of CRC.]. 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:11705868; 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:NP1017841.RAc8DyIoSCWkA-zfg9zA3s8ZJLsOFi1sMfAPDsKkvVhWk130_publicationInfo { this: dcterms:created "2015-08-25T14:48:11+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" . }