Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP294892.RANP480Wcg7tL3nMx11y0No0mVc6QozuB1eanCb38nUps130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP294892.RANP480Wcg7tL3nMx11y0No0mVc6QozuB1eanCb38nUps130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294892.RANP480Wcg7tL3nMx11y0No0mVc6QozuB1eanCb38nUps130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294892.RANP480Wcg7tL3nMx11y0No0mVc6QozuB1eanCb38nUps130_provenance.
- befree-2016 importedOn "2016-02-19" NP294892.RANP480Wcg7tL3nMx11y0No0mVc6QozuB1eanCb38nUps130_provenance.
- NP294892.RANP480Wcg7tL3nMx11y0No0mVc6QozuB1eanCb38nUps130_assertion wasGeneratedBy ECO_0000203 NP294892.RANP480Wcg7tL3nMx11y0No0mVc6QozuB1eanCb38nUps130_provenance.
- NP294892.RANP480Wcg7tL3nMx11y0No0mVc6QozuB1eanCb38nUps130_assertion wasDerivedFrom befree-2016 NP294892.RANP480Wcg7tL3nMx11y0No0mVc6QozuB1eanCb38nUps130_provenance.
- NP294892.RANP480Wcg7tL3nMx11y0No0mVc6QozuB1eanCb38nUps130_assertion SIO_000772 10984082 NP294892.RANP480Wcg7tL3nMx11y0No0mVc6QozuB1eanCb38nUps130_provenance.
- NP294892.RANP480Wcg7tL3nMx11y0No0mVc6QozuB1eanCb38nUps130_assertion evidence source_evidence_literature NP294892.RANP480Wcg7tL3nMx11y0No0mVc6QozuB1eanCb38nUps130_provenance.
- NP294892.RANP480Wcg7tL3nMx11y0No0mVc6QozuB1eanCb38nUps130_assertion description "[Familial defective apolipoprotein B-100 (FDB) is a genetic disorder caused by a substitution of glutamine for arginine at residue 3500 of the apolipoprotein B-100 molecule.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294892.RANP480Wcg7tL3nMx11y0No0mVc6QozuB1eanCb38nUps130_provenance.