Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP4103.RA3khij8tfpPoWIrG2cIX3zbmnS5Illh6o2NW0UwlcDyA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP4103.RA3khij8tfpPoWIrG2cIX3zbmnS5Illh6o2NW0UwlcDyA130_assertion type Assertion NP4103.RA3khij8tfpPoWIrG2cIX3zbmnS5Illh6o2NW0UwlcDyA130_head.
- 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.