Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP817542.RASpJLLpQ4jmjb5_QxFP4iudW__vE-zgJhz4isSdvJfYc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP817542.RASpJLLpQ4jmjb5_QxFP4iudW__vE-zgJhz4isSdvJfYc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP817542.RASpJLLpQ4jmjb5_QxFP4iudW__vE-zgJhz4isSdvJfYc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP817542.RASpJLLpQ4jmjb5_QxFP4iudW__vE-zgJhz4isSdvJfYc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP817542.RASpJLLpQ4jmjb5_QxFP4iudW__vE-zgJhz4isSdvJfYc130_provenance.
- NP817542.RASpJLLpQ4jmjb5_QxFP4iudW__vE-zgJhz4isSdvJfYc130_assertion wasGeneratedBy ECO_0000203 NP817542.RASpJLLpQ4jmjb5_QxFP4iudW__vE-zgJhz4isSdvJfYc130_provenance.
- NP817542.RASpJLLpQ4jmjb5_QxFP4iudW__vE-zgJhz4isSdvJfYc130_assertion wasDerivedFrom befree-20150227 NP817542.RASpJLLpQ4jmjb5_QxFP4iudW__vE-zgJhz4isSdvJfYc130_provenance.
- NP817542.RASpJLLpQ4jmjb5_QxFP4iudW__vE-zgJhz4isSdvJfYc130_assertion SIO_000772 19298753 NP817542.RASpJLLpQ4jmjb5_QxFP4iudW__vE-zgJhz4isSdvJfYc130_provenance.
- NP817542.RASpJLLpQ4jmjb5_QxFP4iudW__vE-zgJhz4isSdvJfYc130_assertion evidence source_evidence_literature NP817542.RASpJLLpQ4jmjb5_QxFP4iudW__vE-zgJhz4isSdvJfYc130_provenance.
- NP817542.RASpJLLpQ4jmjb5_QxFP4iudW__vE-zgJhz4isSdvJfYc130_assertion description "[In addition, mutations of leucine-rich, glioma-inactivated 1 gene leads to genetic abnormalities of familial lateral temporal lobe epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP817542.RASpJLLpQ4jmjb5_QxFP4iudW__vE-zgJhz4isSdvJfYc130_provenance.