Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1036708.RAqxUH2qmoQiqcysxIHJ6K7E1GbdLsSetveMq8FxUXR4Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1036708.RAqxUH2qmoQiqcysxIHJ6K7E1GbdLsSetveMq8FxUXR4Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1036708.RAqxUH2qmoQiqcysxIHJ6K7E1GbdLsSetveMq8FxUXR4Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1036708.RAqxUH2qmoQiqcysxIHJ6K7E1GbdLsSetveMq8FxUXR4Q130_provenance.
- NP1036708.RAqxUH2qmoQiqcysxIHJ6K7E1GbdLsSetveMq8FxUXR4Q130_assertion description "[Polyalanine (polyA)-expansion-encoding mutations of aristaless-related homeobox (ARX) cause a spectrum of X-linked ID (XLID) diseases and chronic epilepsy, including infantile spasms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1036708.RAqxUH2qmoQiqcysxIHJ6K7E1GbdLsSetveMq8FxUXR4Q130_provenance.
- NP1036708.RAqxUH2qmoQiqcysxIHJ6K7E1GbdLsSetveMq8FxUXR4Q130_assertion evidence source_evidence_literature NP1036708.RAqxUH2qmoQiqcysxIHJ6K7E1GbdLsSetveMq8FxUXR4Q130_provenance.
- NP1036708.RAqxUH2qmoQiqcysxIHJ6K7E1GbdLsSetveMq8FxUXR4Q130_assertion SIO_000772 23246292 NP1036708.RAqxUH2qmoQiqcysxIHJ6K7E1GbdLsSetveMq8FxUXR4Q130_provenance.
- NP1036708.RAqxUH2qmoQiqcysxIHJ6K7E1GbdLsSetveMq8FxUXR4Q130_assertion wasDerivedFrom befree-2016 NP1036708.RAqxUH2qmoQiqcysxIHJ6K7E1GbdLsSetveMq8FxUXR4Q130_provenance.
- NP1036708.RAqxUH2qmoQiqcysxIHJ6K7E1GbdLsSetveMq8FxUXR4Q130_assertion wasGeneratedBy ECO_0000203 NP1036708.RAqxUH2qmoQiqcysxIHJ6K7E1GbdLsSetveMq8FxUXR4Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP1036708.RAqxUH2qmoQiqcysxIHJ6K7E1GbdLsSetveMq8FxUXR4Q130_provenance.