Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP230560.RAUGrqGqixZby7P1kFjbAuxqRvYBW8twtApgYA_LX-SvA130_assertion> ?p ?o ?g. }
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- NP230560.RAUGrqGqixZby7P1kFjbAuxqRvYBW8twtApgYA_LX-SvA130_assertion type Assertion NP230560.RAUGrqGqixZby7P1kFjbAuxqRvYBW8twtApgYA_LX-SvA130_head.
- NP230560.RAUGrqGqixZby7P1kFjbAuxqRvYBW8twtApgYA_LX-SvA130_assertion description "[Homozygous loss-of-function PROK2 mutations cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230560.RAUGrqGqixZby7P1kFjbAuxqRvYBW8twtApgYA_LX-SvA130_provenance.
- NP230560.RAUGrqGqixZby7P1kFjbAuxqRvYBW8twtApgYA_LX-SvA130_assertion evidence source_evidence_literature NP230560.RAUGrqGqixZby7P1kFjbAuxqRvYBW8twtApgYA_LX-SvA130_provenance.
- NP230560.RAUGrqGqixZby7P1kFjbAuxqRvYBW8twtApgYA_LX-SvA130_assertion SIO_000772 17959774 NP230560.RAUGrqGqixZby7P1kFjbAuxqRvYBW8twtApgYA_LX-SvA130_provenance.
- NP230560.RAUGrqGqixZby7P1kFjbAuxqRvYBW8twtApgYA_LX-SvA130_assertion wasDerivedFrom lhgdn-20090331 NP230560.RAUGrqGqixZby7P1kFjbAuxqRvYBW8twtApgYA_LX-SvA130_provenance.
- NP230560.RAUGrqGqixZby7P1kFjbAuxqRvYBW8twtApgYA_LX-SvA130_assertion wasGeneratedBy ECO_0000203 NP230560.RAUGrqGqixZby7P1kFjbAuxqRvYBW8twtApgYA_LX-SvA130_provenance.