Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP932021.RAVF0pfXQx6Tw0_XLlrlrW68_r8QuWuiX79wurSOIW4p4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP932021.RAVF0pfXQx6Tw0_XLlrlrW68_r8QuWuiX79wurSOIW4p4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP932021.RAVF0pfXQx6Tw0_XLlrlrW68_r8QuWuiX79wurSOIW4p4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP932021.RAVF0pfXQx6Tw0_XLlrlrW68_r8QuWuiX79wurSOIW4p4130_provenance.
- NP932021.RAVF0pfXQx6Tw0_XLlrlrW68_r8QuWuiX79wurSOIW4p4130_assertion description "[Mutations of the protocadherin19 gene (PCDH19) cause a female-related epilepsy of variable severity, with or without mental retardation and autistic features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932021.RAVF0pfXQx6Tw0_XLlrlrW68_r8QuWuiX79wurSOIW4p4130_provenance.
- NP932021.RAVF0pfXQx6Tw0_XLlrlrW68_r8QuWuiX79wurSOIW4p4130_assertion evidence source_evidence_literature NP932021.RAVF0pfXQx6Tw0_XLlrlrW68_r8QuWuiX79wurSOIW4p4130_provenance.
- NP932021.RAVF0pfXQx6Tw0_XLlrlrW68_r8QuWuiX79wurSOIW4p4130_assertion SIO_000772 22946748 NP932021.RAVF0pfXQx6Tw0_XLlrlrW68_r8QuWuiX79wurSOIW4p4130_provenance.
- NP932021.RAVF0pfXQx6Tw0_XLlrlrW68_r8QuWuiX79wurSOIW4p4130_assertion wasDerivedFrom befree-20150227 NP932021.RAVF0pfXQx6Tw0_XLlrlrW68_r8QuWuiX79wurSOIW4p4130_provenance.
- NP932021.RAVF0pfXQx6Tw0_XLlrlrW68_r8QuWuiX79wurSOIW4p4130_assertion wasGeneratedBy ECO_0000203 NP932021.RAVF0pfXQx6Tw0_XLlrlrW68_r8QuWuiX79wurSOIW4p4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP932021.RAVF0pfXQx6Tw0_XLlrlrW68_r8QuWuiX79wurSOIW4p4130_provenance.