Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP414345.RAw5tHiPeDLe2WcB1f5tg62Dka2ZQNd2SVw31q3hVTrCQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP414345.RAw5tHiPeDLe2WcB1f5tg62Dka2ZQNd2SVw31q3hVTrCQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP414345.RAw5tHiPeDLe2WcB1f5tg62Dka2ZQNd2SVw31q3hVTrCQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP414345.RAw5tHiPeDLe2WcB1f5tg62Dka2ZQNd2SVw31q3hVTrCQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP414345.RAw5tHiPeDLe2WcB1f5tg62Dka2ZQNd2SVw31q3hVTrCQ130_provenance.
- NP414345.RAw5tHiPeDLe2WcB1f5tg62Dka2ZQNd2SVw31q3hVTrCQ130_assertion wasGeneratedBy ECO_0000203 NP414345.RAw5tHiPeDLe2WcB1f5tg62Dka2ZQNd2SVw31q3hVTrCQ130_provenance.
- NP414345.RAw5tHiPeDLe2WcB1f5tg62Dka2ZQNd2SVw31q3hVTrCQ130_assertion wasDerivedFrom befree-20150227 NP414345.RAw5tHiPeDLe2WcB1f5tg62Dka2ZQNd2SVw31q3hVTrCQ130_provenance.
- NP414345.RAw5tHiPeDLe2WcB1f5tg62Dka2ZQNd2SVw31q3hVTrCQ130_assertion SIO_000772 24439481 NP414345.RAw5tHiPeDLe2WcB1f5tg62Dka2ZQNd2SVw31q3hVTrCQ130_provenance.
- NP414345.RAw5tHiPeDLe2WcB1f5tg62Dka2ZQNd2SVw31q3hVTrCQ130_assertion evidence source_evidence_literature NP414345.RAw5tHiPeDLe2WcB1f5tg62Dka2ZQNd2SVw31q3hVTrCQ130_provenance.
- NP414345.RAw5tHiPeDLe2WcB1f5tg62Dka2ZQNd2SVw31q3hVTrCQ130_assertion description "[Mutations in C9ORF72, SOD1, TARDBP, and FUS genes account for approximately two-third of familial cases and 5% of sporadic amyotrophic lateral sclerosis (ALS) cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP414345.RAw5tHiPeDLe2WcB1f5tg62Dka2ZQNd2SVw31q3hVTrCQ130_provenance.