Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP8005.RACc7kj3XVXlvxMRM8UJwGAwph_9le1tHjMCQ4PT-vI28130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP8005.RACc7kj3XVXlvxMRM8UJwGAwph_9le1tHjMCQ4PT-vI28130_assertion type Assertion NP8005.RACc7kj3XVXlvxMRM8UJwGAwph_9le1tHjMCQ4PT-vI28130_head.
- NP8005.RACc7kj3XVXlvxMRM8UJwGAwph_9le1tHjMCQ4PT-vI28130_assertion description "[Mutations in FEZF1 cause Kallmann syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8005.RACc7kj3XVXlvxMRM8UJwGAwph_9le1tHjMCQ4PT-vI28130_provenance.
- NP8005.RACc7kj3XVXlvxMRM8UJwGAwph_9le1tHjMCQ4PT-vI28130_assertion evidence source_evidence_curated NP8005.RACc7kj3XVXlvxMRM8UJwGAwph_9le1tHjMCQ4PT-vI28130_provenance.
- NP8005.RACc7kj3XVXlvxMRM8UJwGAwph_9le1tHjMCQ4PT-vI28130_assertion SIO_000772 25192046 NP8005.RACc7kj3XVXlvxMRM8UJwGAwph_9le1tHjMCQ4PT-vI28130_provenance.
- NP8005.RACc7kj3XVXlvxMRM8UJwGAwph_9le1tHjMCQ4PT-vI28130_assertion wasDerivedFrom uniprot-2016 NP8005.RACc7kj3XVXlvxMRM8UJwGAwph_9le1tHjMCQ4PT-vI28130_provenance.
- NP8005.RACc7kj3XVXlvxMRM8UJwGAwph_9le1tHjMCQ4PT-vI28130_assertion wasGeneratedBy ECO_0000218 NP8005.RACc7kj3XVXlvxMRM8UJwGAwph_9le1tHjMCQ4PT-vI28130_provenance.