Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP854832.RAaXlyIpW1MIdKNaEYg3abjkSP69Wtua4oPif3YIUsBaU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP854832.RAaXlyIpW1MIdKNaEYg3abjkSP69Wtua4oPif3YIUsBaU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP854832.RAaXlyIpW1MIdKNaEYg3abjkSP69Wtua4oPif3YIUsBaU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP854832.RAaXlyIpW1MIdKNaEYg3abjkSP69Wtua4oPif3YIUsBaU130_provenance.
- NP854832.RAaXlyIpW1MIdKNaEYg3abjkSP69Wtua4oPif3YIUsBaU130_assertion description "[Familial Ohtahara syndrome due to a novel ARX gene mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP854832.RAaXlyIpW1MIdKNaEYg3abjkSP69Wtua4oPif3YIUsBaU130_provenance.
- NP854832.RAaXlyIpW1MIdKNaEYg3abjkSP69Wtua4oPif3YIUsBaU130_assertion evidence source_evidence_literature NP854832.RAaXlyIpW1MIdKNaEYg3abjkSP69Wtua4oPif3YIUsBaU130_provenance.
- NP854832.RAaXlyIpW1MIdKNaEYg3abjkSP69Wtua4oPif3YIUsBaU130_assertion SIO_000772 21108397 NP854832.RAaXlyIpW1MIdKNaEYg3abjkSP69Wtua4oPif3YIUsBaU130_provenance.
- NP854832.RAaXlyIpW1MIdKNaEYg3abjkSP69Wtua4oPif3YIUsBaU130_assertion wasDerivedFrom befree-2016 NP854832.RAaXlyIpW1MIdKNaEYg3abjkSP69Wtua4oPif3YIUsBaU130_provenance.
- NP854832.RAaXlyIpW1MIdKNaEYg3abjkSP69Wtua4oPif3YIUsBaU130_assertion wasGeneratedBy ECO_0000203 NP854832.RAaXlyIpW1MIdKNaEYg3abjkSP69Wtua4oPif3YIUsBaU130_provenance.
- befree-2016 importedOn "2016-02-19" NP854832.RAaXlyIpW1MIdKNaEYg3abjkSP69Wtua4oPif3YIUsBaU130_provenance.