Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP237643.RAYEYhS4fgeOlMFcwUM0W8-Dbo2ytv6MG_zJUxCcFlo2s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP237643.RAYEYhS4fgeOlMFcwUM0W8-Dbo2ytv6MG_zJUxCcFlo2s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP237643.RAYEYhS4fgeOlMFcwUM0W8-Dbo2ytv6MG_zJUxCcFlo2s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP237643.RAYEYhS4fgeOlMFcwUM0W8-Dbo2ytv6MG_zJUxCcFlo2s130_provenance.
- NP237643.RAYEYhS4fgeOlMFcwUM0W8-Dbo2ytv6MG_zJUxCcFlo2s130_assertion description "[X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237643.RAYEYhS4fgeOlMFcwUM0W8-Dbo2ytv6MG_zJUxCcFlo2s130_provenance.
- NP237643.RAYEYhS4fgeOlMFcwUM0W8-Dbo2ytv6MG_zJUxCcFlo2s130_assertion evidence source_evidence_literature NP237643.RAYEYhS4fgeOlMFcwUM0W8-Dbo2ytv6MG_zJUxCcFlo2s130_provenance.
- NP237643.RAYEYhS4fgeOlMFcwUM0W8-Dbo2ytv6MG_zJUxCcFlo2s130_assertion SIO_000772 18469813 NP237643.RAYEYhS4fgeOlMFcwUM0W8-Dbo2ytv6MG_zJUxCcFlo2s130_provenance.
- NP237643.RAYEYhS4fgeOlMFcwUM0W8-Dbo2ytv6MG_zJUxCcFlo2s130_assertion wasDerivedFrom lhgdn-20090331 NP237643.RAYEYhS4fgeOlMFcwUM0W8-Dbo2ytv6MG_zJUxCcFlo2s130_provenance.
- NP237643.RAYEYhS4fgeOlMFcwUM0W8-Dbo2ytv6MG_zJUxCcFlo2s130_assertion wasGeneratedBy ECO_0000203 NP237643.RAYEYhS4fgeOlMFcwUM0W8-Dbo2ytv6MG_zJUxCcFlo2s130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP237643.RAYEYhS4fgeOlMFcwUM0W8-Dbo2ytv6MG_zJUxCcFlo2s130_provenance.