Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP147016.RAJgYh18g8cIPMn5ysKh2rSFP3Amq8esh2tNXfP43gl3Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP147016.RAJgYh18g8cIPMn5ysKh2rSFP3Amq8esh2tNXfP43gl3Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP147016.RAJgYh18g8cIPMn5ysKh2rSFP3Amq8esh2tNXfP43gl3Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP147016.RAJgYh18g8cIPMn5ysKh2rSFP3Amq8esh2tNXfP43gl3Y130_provenance.
- NP147016.RAJgYh18g8cIPMn5ysKh2rSFP3Amq8esh2tNXfP43gl3Y130_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." NP147016.RAJgYh18g8cIPMn5ysKh2rSFP3Amq8esh2tNXfP43gl3Y130_provenance.
- NP147016.RAJgYh18g8cIPMn5ysKh2rSFP3Amq8esh2tNXfP43gl3Y130_assertion evidence source_evidence_literature NP147016.RAJgYh18g8cIPMn5ysKh2rSFP3Amq8esh2tNXfP43gl3Y130_provenance.
- NP147016.RAJgYh18g8cIPMn5ysKh2rSFP3Amq8esh2tNXfP43gl3Y130_assertion SIO_000772 17959774 NP147016.RAJgYh18g8cIPMn5ysKh2rSFP3Amq8esh2tNXfP43gl3Y130_provenance.
- NP147016.RAJgYh18g8cIPMn5ysKh2rSFP3Amq8esh2tNXfP43gl3Y130_assertion wasDerivedFrom lhgdn-20090331 NP147016.RAJgYh18g8cIPMn5ysKh2rSFP3Amq8esh2tNXfP43gl3Y130_provenance.
- NP147016.RAJgYh18g8cIPMn5ysKh2rSFP3Amq8esh2tNXfP43gl3Y130_assertion wasGeneratedBy ECO_0000203 NP147016.RAJgYh18g8cIPMn5ysKh2rSFP3Amq8esh2tNXfP43gl3Y130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP147016.RAJgYh18g8cIPMn5ysKh2rSFP3Amq8esh2tNXfP43gl3Y130_provenance.