Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1385027.RALVRDmUWBsI7_RGnOhS8dsxUykgBOI3Rl2JxjX88ETFk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1385027.RALVRDmUWBsI7_RGnOhS8dsxUykgBOI3Rl2JxjX88ETFk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1385027.RALVRDmUWBsI7_RGnOhS8dsxUykgBOI3Rl2JxjX88ETFk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1385027.RALVRDmUWBsI7_RGnOhS8dsxUykgBOI3Rl2JxjX88ETFk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1385027.RALVRDmUWBsI7_RGnOhS8dsxUykgBOI3Rl2JxjX88ETFk130_provenance.
- NP1385027.RALVRDmUWBsI7_RGnOhS8dsxUykgBOI3Rl2JxjX88ETFk130_assertion wasGeneratedBy ECO_0000203 NP1385027.RALVRDmUWBsI7_RGnOhS8dsxUykgBOI3Rl2JxjX88ETFk130_provenance.
- NP1385027.RALVRDmUWBsI7_RGnOhS8dsxUykgBOI3Rl2JxjX88ETFk130_assertion wasDerivedFrom befree-2016 NP1385027.RALVRDmUWBsI7_RGnOhS8dsxUykgBOI3Rl2JxjX88ETFk130_provenance.
- NP1385027.RALVRDmUWBsI7_RGnOhS8dsxUykgBOI3Rl2JxjX88ETFk130_assertion SIO_000772 9393760 NP1385027.RALVRDmUWBsI7_RGnOhS8dsxUykgBOI3Rl2JxjX88ETFk130_provenance.
- NP1385027.RALVRDmUWBsI7_RGnOhS8dsxUykgBOI3Rl2JxjX88ETFk130_assertion evidence source_evidence_literature NP1385027.RALVRDmUWBsI7_RGnOhS8dsxUykgBOI3Rl2JxjX88ETFk130_provenance.
- NP1385027.RALVRDmUWBsI7_RGnOhS8dsxUykgBOI3Rl2JxjX88ETFk130_assertion description "[A homozygous deletion including Hel-N1 and CDKN2a was found in a SCLC cell line, and a single-base polymorphism in exon 2 of Hel-N1 was observed in eight tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1385027.RALVRDmUWBsI7_RGnOhS8dsxUykgBOI3Rl2JxjX88ETFk130_provenance.