Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP3806.RA6t6Dvm_RyP18S92cC95amCpseBH94X0K4aGsSNO6w70130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP3806.RA6t6Dvm_RyP18S92cC95amCpseBH94X0K4aGsSNO6w70130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3806.RA6t6Dvm_RyP18S92cC95amCpseBH94X0K4aGsSNO6w70130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3806.RA6t6Dvm_RyP18S92cC95amCpseBH94X0K4aGsSNO6w70130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP3806.RA6t6Dvm_RyP18S92cC95amCpseBH94X0K4aGsSNO6w70130_provenance.
- NP3806.RA6t6Dvm_RyP18S92cC95amCpseBH94X0K4aGsSNO6w70130_assertion wasGeneratedBy ECO_0000218 NP3806.RA6t6Dvm_RyP18S92cC95amCpseBH94X0K4aGsSNO6w70130_provenance.
- NP3806.RA6t6Dvm_RyP18S92cC95amCpseBH94X0K4aGsSNO6w70130_assertion wasDerivedFrom uniprot-2016 NP3806.RA6t6Dvm_RyP18S92cC95amCpseBH94X0K4aGsSNO6w70130_provenance.
- NP3806.RA6t6Dvm_RyP18S92cC95amCpseBH94X0K4aGsSNO6w70130_assertion SIO_000772 15605412 NP3806.RA6t6Dvm_RyP18S92cC95amCpseBH94X0K4aGsSNO6w70130_provenance.
- NP3806.RA6t6Dvm_RyP18S92cC95amCpseBH94X0K4aGsSNO6w70130_assertion evidence source_evidence_curated NP3806.RA6t6Dvm_RyP18S92cC95amCpseBH94X0K4aGsSNO6w70130_provenance.
- NP3806.RA6t6Dvm_RyP18S92cC95amCpseBH94X0K4aGsSNO6w70130_assertion description "[Kallmann syndrome: 14 novel mutations in KAL1 and FGFR1 (KAL2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3806.RA6t6Dvm_RyP18S92cC95amCpseBH94X0K4aGsSNO6w70130_provenance.