Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP419.RAbkRpnUfFiDUCKQ1c7NBKiXFtfUhTC1gteYTTD47P1Jc130_assertion> ?p ?o ?g. }
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- NP419.RAbkRpnUfFiDUCKQ1c7NBKiXFtfUhTC1gteYTTD47P1Jc130_assertion type Assertion NP419.RAbkRpnUfFiDUCKQ1c7NBKiXFtfUhTC1gteYTTD47P1Jc130_head.
- NP419.RAbkRpnUfFiDUCKQ1c7NBKiXFtfUhTC1gteYTTD47P1Jc130_assertion wasGeneratedBy ECO_0000218 NP419.RAbkRpnUfFiDUCKQ1c7NBKiXFtfUhTC1gteYTTD47P1Jc130_provenance.
- NP419.RAbkRpnUfFiDUCKQ1c7NBKiXFtfUhTC1gteYTTD47P1Jc130_assertion wasDerivedFrom uniprot-20150221 NP419.RAbkRpnUfFiDUCKQ1c7NBKiXFtfUhTC1gteYTTD47P1Jc130_provenance.
- NP419.RAbkRpnUfFiDUCKQ1c7NBKiXFtfUhTC1gteYTTD47P1Jc130_assertion SIO_000772 9462743 NP419.RAbkRpnUfFiDUCKQ1c7NBKiXFtfUhTC1gteYTTD47P1Jc130_provenance.
- NP419.RAbkRpnUfFiDUCKQ1c7NBKiXFtfUhTC1gteYTTD47P1Jc130_assertion evidence source_evidence_curated NP419.RAbkRpnUfFiDUCKQ1c7NBKiXFtfUhTC1gteYTTD47P1Jc130_provenance.
- NP419.RAbkRpnUfFiDUCKQ1c7NBKiXFtfUhTC1gteYTTD47P1Jc130_assertion description "[Mutations in PROP1 cause familial combined pituitary hormone deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP419.RAbkRpnUfFiDUCKQ1c7NBKiXFtfUhTC1gteYTTD47P1Jc130_provenance.