Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP649655.RAUKbUGMeIgn-DcPNvWySdp3v-_1HwlI6YOveoWFwRlnM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP649655.RAUKbUGMeIgn-DcPNvWySdp3v-_1HwlI6YOveoWFwRlnM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP649655.RAUKbUGMeIgn-DcPNvWySdp3v-_1HwlI6YOveoWFwRlnM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP649655.RAUKbUGMeIgn-DcPNvWySdp3v-_1HwlI6YOveoWFwRlnM130_provenance.
- NP649655.RAUKbUGMeIgn-DcPNvWySdp3v-_1HwlI6YOveoWFwRlnM130_assertion description "[These data suggest AMPD2-related PCH as a potentially treatable early-onset neurodegenerative disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP649655.RAUKbUGMeIgn-DcPNvWySdp3v-_1HwlI6YOveoWFwRlnM130_provenance.
- NP649655.RAUKbUGMeIgn-DcPNvWySdp3v-_1HwlI6YOveoWFwRlnM130_assertion evidence source_evidence_literature NP649655.RAUKbUGMeIgn-DcPNvWySdp3v-_1HwlI6YOveoWFwRlnM130_provenance.
- NP649655.RAUKbUGMeIgn-DcPNvWySdp3v-_1HwlI6YOveoWFwRlnM130_assertion SIO_000772 23911318 NP649655.RAUKbUGMeIgn-DcPNvWySdp3v-_1HwlI6YOveoWFwRlnM130_provenance.
- NP649655.RAUKbUGMeIgn-DcPNvWySdp3v-_1HwlI6YOveoWFwRlnM130_assertion wasDerivedFrom befree-20140225 NP649655.RAUKbUGMeIgn-DcPNvWySdp3v-_1HwlI6YOveoWFwRlnM130_provenance.
- NP649655.RAUKbUGMeIgn-DcPNvWySdp3v-_1HwlI6YOveoWFwRlnM130_assertion wasGeneratedBy ECO_0000203 NP649655.RAUKbUGMeIgn-DcPNvWySdp3v-_1HwlI6YOveoWFwRlnM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP649655.RAUKbUGMeIgn-DcPNvWySdp3v-_1HwlI6YOveoWFwRlnM130_provenance.