Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP7486.RAYYk_F1CbSJ3kF732YBSvm0WXINARn9RWvkaoQh5xnhs130_assertion> ?p ?o ?g. }
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- NP7486.RAYYk_F1CbSJ3kF732YBSvm0WXINARn9RWvkaoQh5xnhs130_assertion type Assertion NP7486.RAYYk_F1CbSJ3kF732YBSvm0WXINARn9RWvkaoQh5xnhs130_head.
- NP7486.RAYYk_F1CbSJ3kF732YBSvm0WXINARn9RWvkaoQh5xnhs130_assertion description "[Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7486.RAYYk_F1CbSJ3kF732YBSvm0WXINARn9RWvkaoQh5xnhs130_provenance.
- NP7486.RAYYk_F1CbSJ3kF732YBSvm0WXINARn9RWvkaoQh5xnhs130_assertion evidence source_evidence_curated NP7486.RAYYk_F1CbSJ3kF732YBSvm0WXINARn9RWvkaoQh5xnhs130_provenance.
- NP7486.RAYYk_F1CbSJ3kF732YBSvm0WXINARn9RWvkaoQh5xnhs130_assertion SIO_000772 23643382 NP7486.RAYYk_F1CbSJ3kF732YBSvm0WXINARn9RWvkaoQh5xnhs130_provenance.
- NP7486.RAYYk_F1CbSJ3kF732YBSvm0WXINARn9RWvkaoQh5xnhs130_assertion wasDerivedFrom uniprot-2016 NP7486.RAYYk_F1CbSJ3kF732YBSvm0WXINARn9RWvkaoQh5xnhs130_provenance.
- NP7486.RAYYk_F1CbSJ3kF732YBSvm0WXINARn9RWvkaoQh5xnhs130_assertion wasGeneratedBy ECO_0000218 NP7486.RAYYk_F1CbSJ3kF732YBSvm0WXINARn9RWvkaoQh5xnhs130_provenance.