Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1247486.RAg7fqnPcU9OD3SIts0N0rNrTme6OccN2eS3lTQ7jWTEc130_assertion> ?p ?o ?g. }
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- NP1247486.RAg7fqnPcU9OD3SIts0N0rNrTme6OccN2eS3lTQ7jWTEc130_assertion type Assertion NP1247486.RAg7fqnPcU9OD3SIts0N0rNrTme6OccN2eS3lTQ7jWTEc130_head.
- NP1247486.RAg7fqnPcU9OD3SIts0N0rNrTme6OccN2eS3lTQ7jWTEc130_assertion description "[Mutations in the fibroblast growth factor receptor 1 gene (FGFR1) have been reported in patients with Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism (nIHH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1247486.RAg7fqnPcU9OD3SIts0N0rNrTme6OccN2eS3lTQ7jWTEc130_provenance.
- NP1247486.RAg7fqnPcU9OD3SIts0N0rNrTme6OccN2eS3lTQ7jWTEc130_assertion evidence source_evidence_literature NP1247486.RAg7fqnPcU9OD3SIts0N0rNrTme6OccN2eS3lTQ7jWTEc130_provenance.
- NP1247486.RAg7fqnPcU9OD3SIts0N0rNrTme6OccN2eS3lTQ7jWTEc130_assertion SIO_000772 25501157 NP1247486.RAg7fqnPcU9OD3SIts0N0rNrTme6OccN2eS3lTQ7jWTEc130_provenance.
- NP1247486.RAg7fqnPcU9OD3SIts0N0rNrTme6OccN2eS3lTQ7jWTEc130_assertion wasDerivedFrom befree-2016 NP1247486.RAg7fqnPcU9OD3SIts0N0rNrTme6OccN2eS3lTQ7jWTEc130_provenance.
- NP1247486.RAg7fqnPcU9OD3SIts0N0rNrTme6OccN2eS3lTQ7jWTEc130_assertion wasGeneratedBy ECO_0000203 NP1247486.RAg7fqnPcU9OD3SIts0N0rNrTme6OccN2eS3lTQ7jWTEc130_provenance.