Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP197922.RA5Hg2P2iYQ_ed-I5Om1ZQxmgPwQvMiom68b5J3BarSoM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP197922.RA5Hg2P2iYQ_ed-I5Om1ZQxmgPwQvMiom68b5J3BarSoM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP197922.RA5Hg2P2iYQ_ed-I5Om1ZQxmgPwQvMiom68b5J3BarSoM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP197922.RA5Hg2P2iYQ_ed-I5Om1ZQxmgPwQvMiom68b5J3BarSoM130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP197922.RA5Hg2P2iYQ_ed-I5Om1ZQxmgPwQvMiom68b5J3BarSoM130_provenance.
- NP197922.RA5Hg2P2iYQ_ed-I5Om1ZQxmgPwQvMiom68b5J3BarSoM130_assertion wasGeneratedBy ECO_0000203 NP197922.RA5Hg2P2iYQ_ed-I5Om1ZQxmgPwQvMiom68b5J3BarSoM130_provenance.
- NP197922.RA5Hg2P2iYQ_ed-I5Om1ZQxmgPwQvMiom68b5J3BarSoM130_assertion wasDerivedFrom lhgdn-20090331 NP197922.RA5Hg2P2iYQ_ed-I5Om1ZQxmgPwQvMiom68b5J3BarSoM130_provenance.
- NP197922.RA5Hg2P2iYQ_ed-I5Om1ZQxmgPwQvMiom68b5J3BarSoM130_assertion SIO_000772 12730697 NP197922.RA5Hg2P2iYQ_ed-I5Om1ZQxmgPwQvMiom68b5J3BarSoM130_provenance.
- NP197922.RA5Hg2P2iYQ_ed-I5Om1ZQxmgPwQvMiom68b5J3BarSoM130_assertion evidence source_evidence_literature NP197922.RA5Hg2P2iYQ_ed-I5Om1ZQxmgPwQvMiom68b5J3BarSoM130_provenance.
- NP197922.RA5Hg2P2iYQ_ed-I5Om1ZQxmgPwQvMiom68b5J3BarSoM130_assertion description "[two mutations in the gene PCSK9 (encoding proprotein convertase subtilisin/kexin type 9) that cause autosomal dominant hypercholesterolemia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP197922.RA5Hg2P2iYQ_ed-I5Om1ZQxmgPwQvMiom68b5J3BarSoM130_provenance.