Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP201919.RA0RZ1pFvL61zW4yLulHJpATGv6LPSHYTuk2wvCUjsPeM130_assertion> ?p ?o ?g. }
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- NP201919.RA0RZ1pFvL61zW4yLulHJpATGv6LPSHYTuk2wvCUjsPeM130_assertion type Assertion NP201919.RA0RZ1pFvL61zW4yLulHJpATGv6LPSHYTuk2wvCUjsPeM130_head.
- NP201919.RA0RZ1pFvL61zW4yLulHJpATGv6LPSHYTuk2wvCUjsPeM130_assertion description "[Mutations in GPR54 cause autosomal recessive idiopathic hypogonadotropic hypogonadism in humans and mice, suggesting that this receptor is essential for normal gonadotropin-releasing hormone physiology and for puberty.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP201919.RA0RZ1pFvL61zW4yLulHJpATGv6LPSHYTuk2wvCUjsPeM130_provenance.
- NP201919.RA0RZ1pFvL61zW4yLulHJpATGv6LPSHYTuk2wvCUjsPeM130_assertion evidence source_evidence_literature NP201919.RA0RZ1pFvL61zW4yLulHJpATGv6LPSHYTuk2wvCUjsPeM130_provenance.
- NP201919.RA0RZ1pFvL61zW4yLulHJpATGv6LPSHYTuk2wvCUjsPeM130_assertion SIO_000772 14573733 NP201919.RA0RZ1pFvL61zW4yLulHJpATGv6LPSHYTuk2wvCUjsPeM130_provenance.
- NP201919.RA0RZ1pFvL61zW4yLulHJpATGv6LPSHYTuk2wvCUjsPeM130_assertion wasDerivedFrom lhgdn-20090331 NP201919.RA0RZ1pFvL61zW4yLulHJpATGv6LPSHYTuk2wvCUjsPeM130_provenance.
- NP201919.RA0RZ1pFvL61zW4yLulHJpATGv6LPSHYTuk2wvCUjsPeM130_assertion wasGeneratedBy ECO_0000203 NP201919.RA0RZ1pFvL61zW4yLulHJpATGv6LPSHYTuk2wvCUjsPeM130_provenance.