Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP416265.RA3mmRnlXcAvg97CMvMAaI5nKvK2VwzYdrmEwuvoSMZtE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP416265.RA3mmRnlXcAvg97CMvMAaI5nKvK2VwzYdrmEwuvoSMZtE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP416265.RA3mmRnlXcAvg97CMvMAaI5nKvK2VwzYdrmEwuvoSMZtE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP416265.RA3mmRnlXcAvg97CMvMAaI5nKvK2VwzYdrmEwuvoSMZtE130_provenance.
- NP416265.RA3mmRnlXcAvg97CMvMAaI5nKvK2VwzYdrmEwuvoSMZtE130_assertion description "[Severe generalized dystonia as a presentation of a patient with aprataxin gene mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP416265.RA3mmRnlXcAvg97CMvMAaI5nKvK2VwzYdrmEwuvoSMZtE130_provenance.
- NP416265.RA3mmRnlXcAvg97CMvMAaI5nKvK2VwzYdrmEwuvoSMZtE130_assertion evidence source_evidence_literature NP416265.RA3mmRnlXcAvg97CMvMAaI5nKvK2VwzYdrmEwuvoSMZtE130_provenance.
- NP416265.RA3mmRnlXcAvg97CMvMAaI5nKvK2VwzYdrmEwuvoSMZtE130_assertion SIO_000772 14534929 NP416265.RA3mmRnlXcAvg97CMvMAaI5nKvK2VwzYdrmEwuvoSMZtE130_provenance.
- NP416265.RA3mmRnlXcAvg97CMvMAaI5nKvK2VwzYdrmEwuvoSMZtE130_assertion wasDerivedFrom befree-2016 NP416265.RA3mmRnlXcAvg97CMvMAaI5nKvK2VwzYdrmEwuvoSMZtE130_provenance.
- NP416265.RA3mmRnlXcAvg97CMvMAaI5nKvK2VwzYdrmEwuvoSMZtE130_assertion wasGeneratedBy ECO_0000203 NP416265.RA3mmRnlXcAvg97CMvMAaI5nKvK2VwzYdrmEwuvoSMZtE130_provenance.
- befree-2016 importedOn "2016-02-19" NP416265.RA3mmRnlXcAvg97CMvMAaI5nKvK2VwzYdrmEwuvoSMZtE130_provenance.