Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP637062.RAXs6jv1Zb1eSMCr_5lcYlJ7Kr7wxsrjQBJvcY5297Cz8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP637062.RAXs6jv1Zb1eSMCr_5lcYlJ7Kr7wxsrjQBJvcY5297Cz8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP637062.RAXs6jv1Zb1eSMCr_5lcYlJ7Kr7wxsrjQBJvcY5297Cz8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP637062.RAXs6jv1Zb1eSMCr_5lcYlJ7Kr7wxsrjQBJvcY5297Cz8130_provenance.
- NP637062.RAXs6jv1Zb1eSMCr_5lcYlJ7Kr7wxsrjQBJvcY5297Cz8130_assertion description "[Loss-of-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP637062.RAXs6jv1Zb1eSMCr_5lcYlJ7Kr7wxsrjQBJvcY5297Cz8130_provenance.
- NP637062.RAXs6jv1Zb1eSMCr_5lcYlJ7Kr7wxsrjQBJvcY5297Cz8130_assertion evidence source_evidence_literature NP637062.RAXs6jv1Zb1eSMCr_5lcYlJ7Kr7wxsrjQBJvcY5297Cz8130_provenance.
- NP637062.RAXs6jv1Zb1eSMCr_5lcYlJ7Kr7wxsrjQBJvcY5297Cz8130_assertion SIO_000772 17959774 NP637062.RAXs6jv1Zb1eSMCr_5lcYlJ7Kr7wxsrjQBJvcY5297Cz8130_provenance.
- NP637062.RAXs6jv1Zb1eSMCr_5lcYlJ7Kr7wxsrjQBJvcY5297Cz8130_assertion wasDerivedFrom befree-2016 NP637062.RAXs6jv1Zb1eSMCr_5lcYlJ7Kr7wxsrjQBJvcY5297Cz8130_provenance.
- NP637062.RAXs6jv1Zb1eSMCr_5lcYlJ7Kr7wxsrjQBJvcY5297Cz8130_assertion wasGeneratedBy ECO_0000203 NP637062.RAXs6jv1Zb1eSMCr_5lcYlJ7Kr7wxsrjQBJvcY5297Cz8130_provenance.
- befree-2016 importedOn "2016-02-19" NP637062.RAXs6jv1Zb1eSMCr_5lcYlJ7Kr7wxsrjQBJvcY5297Cz8130_provenance.