Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP235904.RAmc_kaReY-2-sErHNeOPNmOOec3WEXgadx691QPNw0mU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP235904.RAmc_kaReY-2-sErHNeOPNmOOec3WEXgadx691QPNw0mU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP235904.RAmc_kaReY-2-sErHNeOPNmOOec3WEXgadx691QPNw0mU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP235904.RAmc_kaReY-2-sErHNeOPNmOOec3WEXgadx691QPNw0mU130_provenance.
- NP235904.RAmc_kaReY-2-sErHNeOPNmOOec3WEXgadx691QPNw0mU130_assertion description "[Consistent with effects on these fundamental mechanisms, allelic variants of ALOX12 are associated with diseases including schizophrenia, atherosclerosis, and cancers, but the mechanisms have not been defined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP235904.RAmc_kaReY-2-sErHNeOPNmOOec3WEXgadx691QPNw0mU130_provenance.
- NP235904.RAmc_kaReY-2-sErHNeOPNmOOec3WEXgadx691QPNw0mU130_assertion evidence source_evidence_literature NP235904.RAmc_kaReY-2-sErHNeOPNmOOec3WEXgadx691QPNw0mU130_provenance.
- NP235904.RAmc_kaReY-2-sErHNeOPNmOOec3WEXgadx691QPNw0mU130_assertion SIO_000772 24686056 NP235904.RAmc_kaReY-2-sErHNeOPNmOOec3WEXgadx691QPNw0mU130_provenance.
- NP235904.RAmc_kaReY-2-sErHNeOPNmOOec3WEXgadx691QPNw0mU130_assertion wasDerivedFrom befree-20150227 NP235904.RAmc_kaReY-2-sErHNeOPNmOOec3WEXgadx691QPNw0mU130_provenance.
- NP235904.RAmc_kaReY-2-sErHNeOPNmOOec3WEXgadx691QPNw0mU130_assertion wasGeneratedBy ECO_0000203 NP235904.RAmc_kaReY-2-sErHNeOPNmOOec3WEXgadx691QPNw0mU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP235904.RAmc_kaReY-2-sErHNeOPNmOOec3WEXgadx691QPNw0mU130_provenance.