Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP2677.RAHVrJosu70VIW_oPppoqU2sn1dTjyJ9i4Lli8Yhb30F4130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP2677.RAHVrJosu70VIW_oPppoqU2sn1dTjyJ9i4Lli8Yhb30F4130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP2677.RAHVrJosu70VIW_oPppoqU2sn1dTjyJ9i4Lli8Yhb30F4130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP2677.RAHVrJosu70VIW_oPppoqU2sn1dTjyJ9i4Lli8Yhb30F4130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP2677.RAHVrJosu70VIW_oPppoqU2sn1dTjyJ9i4Lli8Yhb30F4130_provenance.
- NP2677.RAHVrJosu70VIW_oPppoqU2sn1dTjyJ9i4Lli8Yhb30F4130_assertion wasGeneratedBy ECO_0000218 NP2677.RAHVrJosu70VIW_oPppoqU2sn1dTjyJ9i4Lli8Yhb30F4130_provenance.
- NP2677.RAHVrJosu70VIW_oPppoqU2sn1dTjyJ9i4Lli8Yhb30F4130_assertion wasDerivedFrom uniprot-2016 NP2677.RAHVrJosu70VIW_oPppoqU2sn1dTjyJ9i4Lli8Yhb30F4130_provenance.
- NP2677.RAHVrJosu70VIW_oPppoqU2sn1dTjyJ9i4Lli8Yhb30F4130_assertion SIO_000772 12730697 NP2677.RAHVrJosu70VIW_oPppoqU2sn1dTjyJ9i4Lli8Yhb30F4130_provenance.
- NP2677.RAHVrJosu70VIW_oPppoqU2sn1dTjyJ9i4Lli8Yhb30F4130_assertion evidence source_evidence_curated NP2677.RAHVrJosu70VIW_oPppoqU2sn1dTjyJ9i4Lli8Yhb30F4130_provenance.
- NP2677.RAHVrJosu70VIW_oPppoqU2sn1dTjyJ9i4Lli8Yhb30F4130_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." NP2677.RAHVrJosu70VIW_oPppoqU2sn1dTjyJ9i4Lli8Yhb30F4130_provenance.