Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP2161.RAxexh6Dk9lr71e8hUD3zdXf4aAN1YVDIfaPVTvy9uKkY130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP2161.RAxexh6Dk9lr71e8hUD3zdXf4aAN1YVDIfaPVTvy9uKkY130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP2161.RAxexh6Dk9lr71e8hUD3zdXf4aAN1YVDIfaPVTvy9uKkY130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP2161.RAxexh6Dk9lr71e8hUD3zdXf4aAN1YVDIfaPVTvy9uKkY130_provenance.
- NP2161.RAxexh6Dk9lr71e8hUD3zdXf4aAN1YVDIfaPVTvy9uKkY130_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." NP2161.RAxexh6Dk9lr71e8hUD3zdXf4aAN1YVDIfaPVTvy9uKkY130_provenance.
- NP2161.RAxexh6Dk9lr71e8hUD3zdXf4aAN1YVDIfaPVTvy9uKkY130_assertion evidence source_evidence_curated NP2161.RAxexh6Dk9lr71e8hUD3zdXf4aAN1YVDIfaPVTvy9uKkY130_provenance.
- NP2161.RAxexh6Dk9lr71e8hUD3zdXf4aAN1YVDIfaPVTvy9uKkY130_assertion SIO_000772 23643382 NP2161.RAxexh6Dk9lr71e8hUD3zdXf4aAN1YVDIfaPVTvy9uKkY130_provenance.
- NP2161.RAxexh6Dk9lr71e8hUD3zdXf4aAN1YVDIfaPVTvy9uKkY130_assertion wasDerivedFrom uniprot-20150221 NP2161.RAxexh6Dk9lr71e8hUD3zdXf4aAN1YVDIfaPVTvy9uKkY130_provenance.
- NP2161.RAxexh6Dk9lr71e8hUD3zdXf4aAN1YVDIfaPVTvy9uKkY130_assertion wasGeneratedBy ECO_0000218 NP2161.RAxexh6Dk9lr71e8hUD3zdXf4aAN1YVDIfaPVTvy9uKkY130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP2161.RAxexh6Dk9lr71e8hUD3zdXf4aAN1YVDIfaPVTvy9uKkY130_provenance.