Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP4103.RA3khij8tfpPoWIrG2cIX3zbmnS5Illh6o2NW0UwlcDyA130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP4103.RA3khij8tfpPoWIrG2cIX3zbmnS5Illh6o2NW0UwlcDyA130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4103.RA3khij8tfpPoWIrG2cIX3zbmnS5Illh6o2NW0UwlcDyA130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4103.RA3khij8tfpPoWIrG2cIX3zbmnS5Illh6o2NW0UwlcDyA130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP4103.RA3khij8tfpPoWIrG2cIX3zbmnS5Illh6o2NW0UwlcDyA130_provenance.
- NP4103.RA3khij8tfpPoWIrG2cIX3zbmnS5Illh6o2NW0UwlcDyA130_assertion wasGeneratedBy ECO_0000218 NP4103.RA3khij8tfpPoWIrG2cIX3zbmnS5Illh6o2NW0UwlcDyA130_provenance.
- NP4103.RA3khij8tfpPoWIrG2cIX3zbmnS5Illh6o2NW0UwlcDyA130_assertion wasDerivedFrom uniprot-20150221 NP4103.RA3khij8tfpPoWIrG2cIX3zbmnS5Illh6o2NW0UwlcDyA130_provenance.
- NP4103.RA3khij8tfpPoWIrG2cIX3zbmnS5Illh6o2NW0UwlcDyA130_assertion SIO_000772 12730697 NP4103.RA3khij8tfpPoWIrG2cIX3zbmnS5Illh6o2NW0UwlcDyA130_provenance.
- NP4103.RA3khij8tfpPoWIrG2cIX3zbmnS5Illh6o2NW0UwlcDyA130_assertion evidence source_evidence_curated NP4103.RA3khij8tfpPoWIrG2cIX3zbmnS5Illh6o2NW0UwlcDyA130_provenance.
- NP4103.RA3khij8tfpPoWIrG2cIX3zbmnS5Illh6o2NW0UwlcDyA130_assertion description "[We mapped a third locus associated with ADH, HCHOLA3 at 1p32, and now report two mutations in the gene PCSK9 (encoding proprotein convertase subtilisin/kexin type 9) that cause ADH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4103.RA3khij8tfpPoWIrG2cIX3zbmnS5Illh6o2NW0UwlcDyA130_provenance.