Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP3748.RAdq9lOWK5JZd0tGbbC4CLaKyn0dJZ5GQ3yVqTOXGvNRE130_assertion> ?p ?o ?g. }
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- NP3748.RAdq9lOWK5JZd0tGbbC4CLaKyn0dJZ5GQ3yVqTOXGvNRE130_assertion type Assertion NP3748.RAdq9lOWK5JZd0tGbbC4CLaKyn0dJZ5GQ3yVqTOXGvNRE130_head.
- NP3748.RAdq9lOWK5JZd0tGbbC4CLaKyn0dJZ5GQ3yVqTOXGvNRE130_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." NP3748.RAdq9lOWK5JZd0tGbbC4CLaKyn0dJZ5GQ3yVqTOXGvNRE130_provenance.
- NP3748.RAdq9lOWK5JZd0tGbbC4CLaKyn0dJZ5GQ3yVqTOXGvNRE130_assertion evidence source_evidence_curated NP3748.RAdq9lOWK5JZd0tGbbC4CLaKyn0dJZ5GQ3yVqTOXGvNRE130_provenance.
- NP3748.RAdq9lOWK5JZd0tGbbC4CLaKyn0dJZ5GQ3yVqTOXGvNRE130_assertion SIO_000772 23643382 NP3748.RAdq9lOWK5JZd0tGbbC4CLaKyn0dJZ5GQ3yVqTOXGvNRE130_provenance.
- NP3748.RAdq9lOWK5JZd0tGbbC4CLaKyn0dJZ5GQ3yVqTOXGvNRE130_assertion wasDerivedFrom uniprot-20150221 NP3748.RAdq9lOWK5JZd0tGbbC4CLaKyn0dJZ5GQ3yVqTOXGvNRE130_provenance.
- NP3748.RAdq9lOWK5JZd0tGbbC4CLaKyn0dJZ5GQ3yVqTOXGvNRE130_assertion wasGeneratedBy ECO_0000218 NP3748.RAdq9lOWK5JZd0tGbbC4CLaKyn0dJZ5GQ3yVqTOXGvNRE130_provenance.