Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP4620.RAjooQ3hv9H9IcWRAKt3kFhkO4OH1ZfnDSuXEXYCP0ufg130_assertion> ?p ?o ?g. }
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- NP4620.RAjooQ3hv9H9IcWRAKt3kFhkO4OH1ZfnDSuXEXYCP0ufg130_assertion type Assertion NP4620.RAjooQ3hv9H9IcWRAKt3kFhkO4OH1ZfnDSuXEXYCP0ufg130_head.
- NP4620.RAjooQ3hv9H9IcWRAKt3kFhkO4OH1ZfnDSuXEXYCP0ufg130_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." NP4620.RAjooQ3hv9H9IcWRAKt3kFhkO4OH1ZfnDSuXEXYCP0ufg130_provenance.
- NP4620.RAjooQ3hv9H9IcWRAKt3kFhkO4OH1ZfnDSuXEXYCP0ufg130_assertion evidence source_evidence_curated NP4620.RAjooQ3hv9H9IcWRAKt3kFhkO4OH1ZfnDSuXEXYCP0ufg130_provenance.
- NP4620.RAjooQ3hv9H9IcWRAKt3kFhkO4OH1ZfnDSuXEXYCP0ufg130_assertion SIO_000772 23643382 NP4620.RAjooQ3hv9H9IcWRAKt3kFhkO4OH1ZfnDSuXEXYCP0ufg130_provenance.
- NP4620.RAjooQ3hv9H9IcWRAKt3kFhkO4OH1ZfnDSuXEXYCP0ufg130_assertion wasDerivedFrom uniprot-20150221 NP4620.RAjooQ3hv9H9IcWRAKt3kFhkO4OH1ZfnDSuXEXYCP0ufg130_provenance.
- NP4620.RAjooQ3hv9H9IcWRAKt3kFhkO4OH1ZfnDSuXEXYCP0ufg130_assertion wasGeneratedBy ECO_0000218 NP4620.RAjooQ3hv9H9IcWRAKt3kFhkO4OH1ZfnDSuXEXYCP0ufg130_provenance.