Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP585137.RAS62mCfaykRaL3HTJzQVpL3hOLsUgJbBAxj0Cd1HyHNA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP585137.RAS62mCfaykRaL3HTJzQVpL3hOLsUgJbBAxj0Cd1HyHNA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP585137.RAS62mCfaykRaL3HTJzQVpL3hOLsUgJbBAxj0Cd1HyHNA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP585137.RAS62mCfaykRaL3HTJzQVpL3hOLsUgJbBAxj0Cd1HyHNA130_provenance.
- NP585137.RAS62mCfaykRaL3HTJzQVpL3hOLsUgJbBAxj0Cd1HyHNA130_assertion description "[The data from this study show overall risk modulation of BCC by variant allele for T241M polymorphism in XRCC3 and gender-specific effect by E185Q polymorphism in NBS1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP585137.RAS62mCfaykRaL3HTJzQVpL3hOLsUgJbBAxj0Cd1HyHNA130_provenance.
- NP585137.RAS62mCfaykRaL3HTJzQVpL3hOLsUgJbBAxj0Cd1HyHNA130_assertion evidence source_evidence_literature NP585137.RAS62mCfaykRaL3HTJzQVpL3hOLsUgJbBAxj0Cd1HyHNA130_provenance.
- NP585137.RAS62mCfaykRaL3HTJzQVpL3hOLsUgJbBAxj0Cd1HyHNA130_assertion SIO_000772 16501254 NP585137.RAS62mCfaykRaL3HTJzQVpL3hOLsUgJbBAxj0Cd1HyHNA130_provenance.
- NP585137.RAS62mCfaykRaL3HTJzQVpL3hOLsUgJbBAxj0Cd1HyHNA130_assertion wasDerivedFrom befree-20150227 NP585137.RAS62mCfaykRaL3HTJzQVpL3hOLsUgJbBAxj0Cd1HyHNA130_provenance.
- NP585137.RAS62mCfaykRaL3HTJzQVpL3hOLsUgJbBAxj0Cd1HyHNA130_assertion wasGeneratedBy ECO_0000203 NP585137.RAS62mCfaykRaL3HTJzQVpL3hOLsUgJbBAxj0Cd1HyHNA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP585137.RAS62mCfaykRaL3HTJzQVpL3hOLsUgJbBAxj0Cd1HyHNA130_provenance.