Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP354682.RAVpWS6vLs1cegkmwA32nSNh1nRH6riijC7qwux304_w8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP354682.RAVpWS6vLs1cegkmwA32nSNh1nRH6riijC7qwux304_w8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP354682.RAVpWS6vLs1cegkmwA32nSNh1nRH6riijC7qwux304_w8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP354682.RAVpWS6vLs1cegkmwA32nSNh1nRH6riijC7qwux304_w8130_provenance.
- NP354682.RAVpWS6vLs1cegkmwA32nSNh1nRH6riijC7qwux304_w8130_assertion description "[The CYP1B1 V432L homozygous variant was associated with decreased risk of meningioma (odds ratio [OR] = 0.6; 95% CI, 0.3-1.0) but not the other tumor types.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP354682.RAVpWS6vLs1cegkmwA32nSNh1nRH6riijC7qwux304_w8130_provenance.
- NP354682.RAVpWS6vLs1cegkmwA32nSNh1nRH6riijC7qwux304_w8130_assertion evidence source_evidence_literature NP354682.RAVpWS6vLs1cegkmwA32nSNh1nRH6riijC7qwux304_w8130_provenance.
- NP354682.RAVpWS6vLs1cegkmwA32nSNh1nRH6riijC7qwux304_w8130_assertion SIO_000772 16598069 NP354682.RAVpWS6vLs1cegkmwA32nSNh1nRH6riijC7qwux304_w8130_provenance.
- NP354682.RAVpWS6vLs1cegkmwA32nSNh1nRH6riijC7qwux304_w8130_assertion wasDerivedFrom befree-20140225 NP354682.RAVpWS6vLs1cegkmwA32nSNh1nRH6riijC7qwux304_w8130_provenance.
- NP354682.RAVpWS6vLs1cegkmwA32nSNh1nRH6riijC7qwux304_w8130_assertion wasGeneratedBy ECO_0000203 NP354682.RAVpWS6vLs1cegkmwA32nSNh1nRH6riijC7qwux304_w8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP354682.RAVpWS6vLs1cegkmwA32nSNh1nRH6riijC7qwux304_w8130_provenance.