Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP626101.RADG-lJANkhMtvfd7VvsMJ06WwumyzvEhhM95CuwX1dEI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP626101.RADG-lJANkhMtvfd7VvsMJ06WwumyzvEhhM95CuwX1dEI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP626101.RADG-lJANkhMtvfd7VvsMJ06WwumyzvEhhM95CuwX1dEI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP626101.RADG-lJANkhMtvfd7VvsMJ06WwumyzvEhhM95CuwX1dEI130_provenance.
- befree-2016 importedOn "2016-02-19" NP626101.RADG-lJANkhMtvfd7VvsMJ06WwumyzvEhhM95CuwX1dEI130_provenance.
- NP626101.RADG-lJANkhMtvfd7VvsMJ06WwumyzvEhhM95CuwX1dEI130_assertion wasGeneratedBy ECO_0000203 NP626101.RADG-lJANkhMtvfd7VvsMJ06WwumyzvEhhM95CuwX1dEI130_provenance.
- NP626101.RADG-lJANkhMtvfd7VvsMJ06WwumyzvEhhM95CuwX1dEI130_assertion wasDerivedFrom befree-2016 NP626101.RADG-lJANkhMtvfd7VvsMJ06WwumyzvEhhM95CuwX1dEI130_provenance.
- NP626101.RADG-lJANkhMtvfd7VvsMJ06WwumyzvEhhM95CuwX1dEI130_assertion SIO_000772 17710733 NP626101.RADG-lJANkhMtvfd7VvsMJ06WwumyzvEhhM95CuwX1dEI130_provenance.
- NP626101.RADG-lJANkhMtvfd7VvsMJ06WwumyzvEhhM95CuwX1dEI130_assertion evidence source_evidence_literature NP626101.RADG-lJANkhMtvfd7VvsMJ06WwumyzvEhhM95CuwX1dEI130_provenance.
- NP626101.RADG-lJANkhMtvfd7VvsMJ06WwumyzvEhhM95CuwX1dEI130_assertion description "[During the last 10 years, 21 loss-of-function GNRHR mutations have been identified in patients with idiopathic hypogonadotropic hypogonadism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP626101.RADG-lJANkhMtvfd7VvsMJ06WwumyzvEhhM95CuwX1dEI130_provenance.