Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP846385.RAoVTSo4M6kTSxGqV0hj0VvesfrIuAfp0DzNf0rCa0wOc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP846385.RAoVTSo4M6kTSxGqV0hj0VvesfrIuAfp0DzNf0rCa0wOc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP846385.RAoVTSo4M6kTSxGqV0hj0VvesfrIuAfp0DzNf0rCa0wOc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP846385.RAoVTSo4M6kTSxGqV0hj0VvesfrIuAfp0DzNf0rCa0wOc130_provenance.
- NP846385.RAoVTSo4M6kTSxGqV0hj0VvesfrIuAfp0DzNf0rCa0wOc130_assertion description "[No disease causing mutations in the GABBR1 gene were detected in patients with sporadic or familial TLE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP846385.RAoVTSo4M6kTSxGqV0hj0VvesfrIuAfp0DzNf0rCa0wOc130_provenance.
- NP846385.RAoVTSo4M6kTSxGqV0hj0VvesfrIuAfp0DzNf0rCa0wOc130_assertion evidence source_evidence_literature NP846385.RAoVTSo4M6kTSxGqV0hj0VvesfrIuAfp0DzNf0rCa0wOc130_provenance.
- NP846385.RAoVTSo4M6kTSxGqV0hj0VvesfrIuAfp0DzNf0rCa0wOc130_assertion SIO_000772 15799783 NP846385.RAoVTSo4M6kTSxGqV0hj0VvesfrIuAfp0DzNf0rCa0wOc130_provenance.
- NP846385.RAoVTSo4M6kTSxGqV0hj0VvesfrIuAfp0DzNf0rCa0wOc130_assertion wasDerivedFrom befree-20150227 NP846385.RAoVTSo4M6kTSxGqV0hj0VvesfrIuAfp0DzNf0rCa0wOc130_provenance.
- NP846385.RAoVTSo4M6kTSxGqV0hj0VvesfrIuAfp0DzNf0rCa0wOc130_assertion wasGeneratedBy ECO_0000203 NP846385.RAoVTSo4M6kTSxGqV0hj0VvesfrIuAfp0DzNf0rCa0wOc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP846385.RAoVTSo4M6kTSxGqV0hj0VvesfrIuAfp0DzNf0rCa0wOc130_provenance.