Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP2244.RAn9Uc7D5j08PAvOLnV7h3djQqvGvszHFVbDD0qWMH9yw130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP2244.RAn9Uc7D5j08PAvOLnV7h3djQqvGvszHFVbDD0qWMH9yw130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP2244.RAn9Uc7D5j08PAvOLnV7h3djQqvGvszHFVbDD0qWMH9yw130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP2244.RAn9Uc7D5j08PAvOLnV7h3djQqvGvszHFVbDD0qWMH9yw130_provenance.
- NP2244.RAn9Uc7D5j08PAvOLnV7h3djQqvGvszHFVbDD0qWMH9yw130_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." NP2244.RAn9Uc7D5j08PAvOLnV7h3djQqvGvszHFVbDD0qWMH9yw130_provenance.
- NP2244.RAn9Uc7D5j08PAvOLnV7h3djQqvGvszHFVbDD0qWMH9yw130_assertion evidence source_evidence_curated NP2244.RAn9Uc7D5j08PAvOLnV7h3djQqvGvszHFVbDD0qWMH9yw130_provenance.
- NP2244.RAn9Uc7D5j08PAvOLnV7h3djQqvGvszHFVbDD0qWMH9yw130_assertion SIO_000772 23643382 NP2244.RAn9Uc7D5j08PAvOLnV7h3djQqvGvszHFVbDD0qWMH9yw130_provenance.
- NP2244.RAn9Uc7D5j08PAvOLnV7h3djQqvGvszHFVbDD0qWMH9yw130_assertion wasDerivedFrom uniprot-20130724 NP2244.RAn9Uc7D5j08PAvOLnV7h3djQqvGvszHFVbDD0qWMH9yw130_provenance.
- NP2244.RAn9Uc7D5j08PAvOLnV7h3djQqvGvszHFVbDD0qWMH9yw130_assertion wasGeneratedBy ECO_0000218 NP2244.RAn9Uc7D5j08PAvOLnV7h3djQqvGvszHFVbDD0qWMH9yw130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP2244.RAn9Uc7D5j08PAvOLnV7h3djQqvGvszHFVbDD0qWMH9yw130_provenance.