Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP714560.RAdYJz1APSY7xq5XsukfwTPSxIg__HS5pPbbbLe1XQIak130_assertion> ?p ?o ?g. }
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- NP714560.RAdYJz1APSY7xq5XsukfwTPSxIg__HS5pPbbbLe1XQIak130_assertion type Assertion NP714560.RAdYJz1APSY7xq5XsukfwTPSxIg__HS5pPbbbLe1XQIak130_head.
- NP714560.RAdYJz1APSY7xq5XsukfwTPSxIg__HS5pPbbbLe1XQIak130_assertion description "[Various missense mutations in the gene coding for prokineticin receptor 2 (PROKR2), a G-protein-coupled receptor, have been identified in patients with Kallmann syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP714560.RAdYJz1APSY7xq5XsukfwTPSxIg__HS5pPbbbLe1XQIak130_provenance.
- NP714560.RAdYJz1APSY7xq5XsukfwTPSxIg__HS5pPbbbLe1XQIak130_assertion evidence source_evidence_literature NP714560.RAdYJz1APSY7xq5XsukfwTPSxIg__HS5pPbbbLe1XQIak130_provenance.
- NP714560.RAdYJz1APSY7xq5XsukfwTPSxIg__HS5pPbbbLe1XQIak130_assertion SIO_000772 24830383 NP714560.RAdYJz1APSY7xq5XsukfwTPSxIg__HS5pPbbbLe1XQIak130_provenance.
- NP714560.RAdYJz1APSY7xq5XsukfwTPSxIg__HS5pPbbbLe1XQIak130_assertion wasDerivedFrom befree-20150227 NP714560.RAdYJz1APSY7xq5XsukfwTPSxIg__HS5pPbbbLe1XQIak130_provenance.
- NP714560.RAdYJz1APSY7xq5XsukfwTPSxIg__HS5pPbbbLe1XQIak130_assertion wasGeneratedBy ECO_0000203 NP714560.RAdYJz1APSY7xq5XsukfwTPSxIg__HS5pPbbbLe1XQIak130_provenance.