Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP700072.RADGB12s2VJ_LGrEAKzvIhoeTK4Adx5fJizHPAE3KiyrE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP700072.RADGB12s2VJ_LGrEAKzvIhoeTK4Adx5fJizHPAE3KiyrE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP700072.RADGB12s2VJ_LGrEAKzvIhoeTK4Adx5fJizHPAE3KiyrE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP700072.RADGB12s2VJ_LGrEAKzvIhoeTK4Adx5fJizHPAE3KiyrE130_provenance.
- NP700072.RADGB12s2VJ_LGrEAKzvIhoeTK4Adx5fJizHPAE3KiyrE130_assertion description "[We analyzed all 41 coding exons of CHD5 for somatic mutations in 123 primary ovarian cancers as well as 60 primary breast cancers using high-resolution melt analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP700072.RADGB12s2VJ_LGrEAKzvIhoeTK4Adx5fJizHPAE3KiyrE130_provenance.
- NP700072.RADGB12s2VJ_LGrEAKzvIhoeTK4Adx5fJizHPAE3KiyrE130_assertion evidence source_evidence_literature NP700072.RADGB12s2VJ_LGrEAKzvIhoeTK4Adx5fJizHPAE3KiyrE130_provenance.
- NP700072.RADGB12s2VJ_LGrEAKzvIhoeTK4Adx5fJizHPAE3KiyrE130_assertion SIO_000772 18953434 NP700072.RADGB12s2VJ_LGrEAKzvIhoeTK4Adx5fJizHPAE3KiyrE130_provenance.
- NP700072.RADGB12s2VJ_LGrEAKzvIhoeTK4Adx5fJizHPAE3KiyrE130_assertion wasDerivedFrom befree-2016 NP700072.RADGB12s2VJ_LGrEAKzvIhoeTK4Adx5fJizHPAE3KiyrE130_provenance.
- NP700072.RADGB12s2VJ_LGrEAKzvIhoeTK4Adx5fJizHPAE3KiyrE130_assertion wasGeneratedBy ECO_0000203 NP700072.RADGB12s2VJ_LGrEAKzvIhoeTK4Adx5fJizHPAE3KiyrE130_provenance.
- befree-2016 importedOn "2016-02-19" NP700072.RADGB12s2VJ_LGrEAKzvIhoeTK4Adx5fJizHPAE3KiyrE130_provenance.