Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP393513.RArVILu9l6IWwjcn4KQOXmQGfIU4w4dzlSMDO508Fwu-s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP393513.RArVILu9l6IWwjcn4KQOXmQGfIU4w4dzlSMDO508Fwu-s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP393513.RArVILu9l6IWwjcn4KQOXmQGfIU4w4dzlSMDO508Fwu-s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP393513.RArVILu9l6IWwjcn4KQOXmQGfIU4w4dzlSMDO508Fwu-s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP393513.RArVILu9l6IWwjcn4KQOXmQGfIU4w4dzlSMDO508Fwu-s130_provenance.
- NP393513.RArVILu9l6IWwjcn4KQOXmQGfIU4w4dzlSMDO508Fwu-s130_assertion wasGeneratedBy ECO_0000203 NP393513.RArVILu9l6IWwjcn4KQOXmQGfIU4w4dzlSMDO508Fwu-s130_provenance.
- NP393513.RArVILu9l6IWwjcn4KQOXmQGfIU4w4dzlSMDO508Fwu-s130_assertion wasDerivedFrom befree-20150227 NP393513.RArVILu9l6IWwjcn4KQOXmQGfIU4w4dzlSMDO508Fwu-s130_provenance.
- NP393513.RArVILu9l6IWwjcn4KQOXmQGfIU4w4dzlSMDO508Fwu-s130_assertion SIO_000772 15695377 NP393513.RArVILu9l6IWwjcn4KQOXmQGfIU4w4dzlSMDO508Fwu-s130_provenance.
- NP393513.RArVILu9l6IWwjcn4KQOXmQGfIU4w4dzlSMDO508Fwu-s130_assertion evidence source_evidence_literature NP393513.RArVILu9l6IWwjcn4KQOXmQGfIU4w4dzlSMDO508Fwu-s130_provenance.
- NP393513.RArVILu9l6IWwjcn4KQOXmQGfIU4w4dzlSMDO508Fwu-s130_assertion description "[The recent identification of FANCC and FANCG mutations in resected pancreatic tumors selected for loss of heterozygosity on chromosome 9, some of which were present in the germ line DNA, suggests that inactivation of these and other Fanconi complementation group genes may contribute to pancreatic cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP393513.RArVILu9l6IWwjcn4KQOXmQGfIU4w4dzlSMDO508Fwu-s130_provenance.