Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP499392.RAcyGVZfL_Y7zsw4drQTfmga4clV00_CYxYr-bBerr-w8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP499392.RAcyGVZfL_Y7zsw4drQTfmga4clV00_CYxYr-bBerr-w8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP499392.RAcyGVZfL_Y7zsw4drQTfmga4clV00_CYxYr-bBerr-w8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP499392.RAcyGVZfL_Y7zsw4drQTfmga4clV00_CYxYr-bBerr-w8130_provenance.
- NP499392.RAcyGVZfL_Y7zsw4drQTfmga4clV00_CYxYr-bBerr-w8130_assertion description "[In conclusion, mutations in GABRA1, GABRB2 and GABRG2 do not seem to be a major genetic cause of epilepsy with typical and atypical absences in Japanese subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP499392.RAcyGVZfL_Y7zsw4drQTfmga4clV00_CYxYr-bBerr-w8130_provenance.
- NP499392.RAcyGVZfL_Y7zsw4drQTfmga4clV00_CYxYr-bBerr-w8130_assertion evidence source_evidence_literature NP499392.RAcyGVZfL_Y7zsw4drQTfmga4clV00_CYxYr-bBerr-w8130_provenance.
- NP499392.RAcyGVZfL_Y7zsw4drQTfmga4clV00_CYxYr-bBerr-w8130_assertion SIO_000772 15955415 NP499392.RAcyGVZfL_Y7zsw4drQTfmga4clV00_CYxYr-bBerr-w8130_provenance.
- NP499392.RAcyGVZfL_Y7zsw4drQTfmga4clV00_CYxYr-bBerr-w8130_assertion wasDerivedFrom befree-2016 NP499392.RAcyGVZfL_Y7zsw4drQTfmga4clV00_CYxYr-bBerr-w8130_provenance.
- NP499392.RAcyGVZfL_Y7zsw4drQTfmga4clV00_CYxYr-bBerr-w8130_assertion wasGeneratedBy ECO_0000203 NP499392.RAcyGVZfL_Y7zsw4drQTfmga4clV00_CYxYr-bBerr-w8130_provenance.
- befree-2016 importedOn "2016-02-19" NP499392.RAcyGVZfL_Y7zsw4drQTfmga4clV00_CYxYr-bBerr-w8130_provenance.