Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP3748.RAdq9lOWK5JZd0tGbbC4CLaKyn0dJZ5GQ3yVqTOXGvNRE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP3748.RAdq9lOWK5JZd0tGbbC4CLaKyn0dJZ5GQ3yVqTOXGvNRE130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3748.RAdq9lOWK5JZd0tGbbC4CLaKyn0dJZ5GQ3yVqTOXGvNRE130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3748.RAdq9lOWK5JZd0tGbbC4CLaKyn0dJZ5GQ3yVqTOXGvNRE130_provenance.
- 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.
- uniprot-20150221 importedOn "2015-02-21" NP3748.RAdq9lOWK5JZd0tGbbC4CLaKyn0dJZ5GQ3yVqTOXGvNRE130_provenance.