Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP3806.RA6t6Dvm_RyP18S92cC95amCpseBH94X0K4aGsSNO6w70130_assertion> ?p ?o ?g. }
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- NP3806.RA6t6Dvm_RyP18S92cC95amCpseBH94X0K4aGsSNO6w70130_assertion type Assertion NP3806.RA6t6Dvm_RyP18S92cC95amCpseBH94X0K4aGsSNO6w70130_head.
- 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.