Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP364619.RA3Jlg3miQq8PTFvM8zjAc84vPtXRDur6LMea0VscCCdk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP364619.RA3Jlg3miQq8PTFvM8zjAc84vPtXRDur6LMea0VscCCdk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP364619.RA3Jlg3miQq8PTFvM8zjAc84vPtXRDur6LMea0VscCCdk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP364619.RA3Jlg3miQq8PTFvM8zjAc84vPtXRDur6LMea0VscCCdk130_provenance.
- NP364619.RA3Jlg3miQq8PTFvM8zjAc84vPtXRDur6LMea0VscCCdk130_assertion wasGeneratedBy ECO_0000203 NP364619.RA3Jlg3miQq8PTFvM8zjAc84vPtXRDur6LMea0VscCCdk130_provenance.
- NP364619.RA3Jlg3miQq8PTFvM8zjAc84vPtXRDur6LMea0VscCCdk130_assertion wasDerivedFrom befree-20140225 NP364619.RA3Jlg3miQq8PTFvM8zjAc84vPtXRDur6LMea0VscCCdk130_provenance.
- NP364619.RA3Jlg3miQq8PTFvM8zjAc84vPtXRDur6LMea0VscCCdk130_assertion SIO_000772 11297579 NP364619.RA3Jlg3miQq8PTFvM8zjAc84vPtXRDur6LMea0VscCCdk130_provenance.
- NP364619.RA3Jlg3miQq8PTFvM8zjAc84vPtXRDur6LMea0VscCCdk130_assertion evidence source_evidence_literature NP364619.RA3Jlg3miQq8PTFvM8zjAc84vPtXRDur6LMea0VscCCdk130_provenance.
- NP364619.RA3Jlg3miQq8PTFvM8zjAc84vPtXRDur6LMea0VscCCdk130_assertion description "[Taken together, these findings suggest that autosomal genes account for the majority of familial cases of KS, and that unique neuroendocrine phenotypes consistent with some GnRH neuronal migration may exist in these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP364619.RA3Jlg3miQq8PTFvM8zjAc84vPtXRDur6LMea0VscCCdk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP364619.RA3Jlg3miQq8PTFvM8zjAc84vPtXRDur6LMea0VscCCdk130_provenance.