Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP7485.RA3vx8-Owr0N4mu2wK6uONhoSWFGcaFQ7QWcy8-IDqq30130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP7485.RA3vx8-Owr0N4mu2wK6uONhoSWFGcaFQ7QWcy8-IDqq30130_assertion type Assertion NP7485.RA3vx8-Owr0N4mu2wK6uONhoSWFGcaFQ7QWcy8-IDqq30130_head.
- NP7485.RA3vx8-Owr0N4mu2wK6uONhoSWFGcaFQ7QWcy8-IDqq30130_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." NP7485.RA3vx8-Owr0N4mu2wK6uONhoSWFGcaFQ7QWcy8-IDqq30130_provenance.
- NP7485.RA3vx8-Owr0N4mu2wK6uONhoSWFGcaFQ7QWcy8-IDqq30130_assertion evidence source_evidence_curated NP7485.RA3vx8-Owr0N4mu2wK6uONhoSWFGcaFQ7QWcy8-IDqq30130_provenance.
- NP7485.RA3vx8-Owr0N4mu2wK6uONhoSWFGcaFQ7QWcy8-IDqq30130_assertion SIO_000772 23643382 NP7485.RA3vx8-Owr0N4mu2wK6uONhoSWFGcaFQ7QWcy8-IDqq30130_provenance.
- NP7485.RA3vx8-Owr0N4mu2wK6uONhoSWFGcaFQ7QWcy8-IDqq30130_assertion wasDerivedFrom uniprot-2016 NP7485.RA3vx8-Owr0N4mu2wK6uONhoSWFGcaFQ7QWcy8-IDqq30130_provenance.
- NP7485.RA3vx8-Owr0N4mu2wK6uONhoSWFGcaFQ7QWcy8-IDqq30130_assertion wasGeneratedBy ECO_0000218 NP7485.RA3vx8-Owr0N4mu2wK6uONhoSWFGcaFQ7QWcy8-IDqq30130_provenance.