Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP867794.RAQaLGGT1ki0mBpA9K6greF-zU1oFs6mMc8SrEbU31G6Q130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP867794.RAQaLGGT1ki0mBpA9K6greF-zU1oFs6mMc8SrEbU31G6Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP867794.RAQaLGGT1ki0mBpA9K6greF-zU1oFs6mMc8SrEbU31G6Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP867794.RAQaLGGT1ki0mBpA9K6greF-zU1oFs6mMc8SrEbU31G6Q130_provenance.
- NP867794.RAQaLGGT1ki0mBpA9K6greF-zU1oFs6mMc8SrEbU31G6Q130_assertion description "[Two dominantly inherited ataxias linked to chromosome 16q22.1: SCA4 and SCA31 are not allelic.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867794.RAQaLGGT1ki0mBpA9K6greF-zU1oFs6mMc8SrEbU31G6Q130_provenance.
- NP867794.RAQaLGGT1ki0mBpA9K6greF-zU1oFs6mMc8SrEbU31G6Q130_assertion evidence source_evidence_literature NP867794.RAQaLGGT1ki0mBpA9K6greF-zU1oFs6mMc8SrEbU31G6Q130_provenance.
- NP867794.RAQaLGGT1ki0mBpA9K6greF-zU1oFs6mMc8SrEbU31G6Q130_assertion SIO_000772 21267591 NP867794.RAQaLGGT1ki0mBpA9K6greF-zU1oFs6mMc8SrEbU31G6Q130_provenance.
- NP867794.RAQaLGGT1ki0mBpA9K6greF-zU1oFs6mMc8SrEbU31G6Q130_assertion wasDerivedFrom befree-2016 NP867794.RAQaLGGT1ki0mBpA9K6greF-zU1oFs6mMc8SrEbU31G6Q130_provenance.
- NP867794.RAQaLGGT1ki0mBpA9K6greF-zU1oFs6mMc8SrEbU31G6Q130_assertion wasGeneratedBy ECO_0000203 NP867794.RAQaLGGT1ki0mBpA9K6greF-zU1oFs6mMc8SrEbU31G6Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP867794.RAQaLGGT1ki0mBpA9K6greF-zU1oFs6mMc8SrEbU31G6Q130_provenance.