@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:NP1249037.RAB9oPH_G_vJfbEXu72LkX70Tz7FIr0KBsC9h6IVCSe8w130_head { this: np:hasAssertion dgn-np:NP1249037.RAB9oPH_G_vJfbEXu72LkX70Tz7FIr0KBsC9h6IVCSe8w130_assertion; np:hasProvenance dgn-np:NP1249037.RAB9oPH_G_vJfbEXu72LkX70Tz7FIr0KBsC9h6IVCSe8w130_provenance; np:hasPublicationInfo dgn-np:NP1249037.RAB9oPH_G_vJfbEXu72LkX70Tz7FIr0KBsC9h6IVCSe8w130_publicationInfo; a np:Nanopublication . dgn-np:NP1249037.RAB9oPH_G_vJfbEXu72LkX70Tz7FIr0KBsC9h6IVCSe8w130_assertion a np:Assertion . dgn-np:NP1249037.RAB9oPH_G_vJfbEXu72LkX70Tz7FIr0KBsC9h6IVCSe8w130_provenance a np:Provenance . dgn-np:NP1249037.RAB9oPH_G_vJfbEXu72LkX70Tz7FIr0KBsC9h6IVCSe8w130_publicationInfo a np:PublicationInfo . } dgn-np:NP1249037.RAB9oPH_G_vJfbEXu72LkX70Tz7FIr0KBsC9h6IVCSe8w130_assertion { miriam-gene:83742 a ncit:C16612 . lld:C0596263 a ncit:C7057 . dgn-gda:DGNfcfe2f8af81e35cdba1a957699e56a90 sio:SIO_000628 miriam-gene:83742, lld:C0596263; a sio:SIO_001121 . } dgn-np:NP1249037.RAB9oPH_G_vJfbEXu72LkX70Tz7FIr0KBsC9h6IVCSe8w130_provenance { dgn-np:NP1249037.RAB9oPH_G_vJfbEXu72LkX70Tz7FIr0KBsC9h6IVCSe8w130_assertion dcterms:description "[The results suggested that MARVELD1 silencing is an appealing diagnostic biomarker for lung cancer and epigenetic silencing of MARVELD1 gene links with the regulatory mechanism of NMD pathway in lung cancer, which may be required for tumorigenesis.]. 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:25520033; 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:NP1249037.RAB9oPH_G_vJfbEXu72LkX70Tz7FIr0KBsC9h6IVCSe8w130_publicationInfo { this: dcterms:created "2016-05-13T12:51:12+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" . }