Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP213854.RAY-fKwG36f1pIkUWdO3D_IHTa53oBeW8UmbRqTI_Bkco130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP213854.RAY-fKwG36f1pIkUWdO3D_IHTa53oBeW8UmbRqTI_Bkco130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP213854.RAY-fKwG36f1pIkUWdO3D_IHTa53oBeW8UmbRqTI_Bkco130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP213854.RAY-fKwG36f1pIkUWdO3D_IHTa53oBeW8UmbRqTI_Bkco130_provenance.
- NP213854.RAY-fKwG36f1pIkUWdO3D_IHTa53oBeW8UmbRqTI_Bkco130_assertion description "[Mutational analysis of the RSPO1 gene in a 46, XX woman with true hermaphroditism, palmoplantar keratoderma, congenital bilateral corneal opacities, onychodystrophy, and hearing impairment, is reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP213854.RAY-fKwG36f1pIkUWdO3D_IHTa53oBeW8UmbRqTI_Bkco130_provenance.
- NP213854.RAY-fKwG36f1pIkUWdO3D_IHTa53oBeW8UmbRqTI_Bkco130_assertion evidence source_evidence_literature NP213854.RAY-fKwG36f1pIkUWdO3D_IHTa53oBeW8UmbRqTI_Bkco130_provenance.
- NP213854.RAY-fKwG36f1pIkUWdO3D_IHTa53oBeW8UmbRqTI_Bkco130_assertion SIO_000772 18085567 NP213854.RAY-fKwG36f1pIkUWdO3D_IHTa53oBeW8UmbRqTI_Bkco130_provenance.
- NP213854.RAY-fKwG36f1pIkUWdO3D_IHTa53oBeW8UmbRqTI_Bkco130_assertion wasDerivedFrom lhgdn-20090331 NP213854.RAY-fKwG36f1pIkUWdO3D_IHTa53oBeW8UmbRqTI_Bkco130_provenance.
- NP213854.RAY-fKwG36f1pIkUWdO3D_IHTa53oBeW8UmbRqTI_Bkco130_assertion wasGeneratedBy ECO_0000203 NP213854.RAY-fKwG36f1pIkUWdO3D_IHTa53oBeW8UmbRqTI_Bkco130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP213854.RAY-fKwG36f1pIkUWdO3D_IHTa53oBeW8UmbRqTI_Bkco130_provenance.