Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP414345.RAw5tHiPeDLe2WcB1f5tg62Dka2ZQNd2SVw31q3hVTrCQ130_assertion> ?p ?o ?g. }
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- NP414345.RAw5tHiPeDLe2WcB1f5tg62Dka2ZQNd2SVw31q3hVTrCQ130_assertion type Assertion NP414345.RAw5tHiPeDLe2WcB1f5tg62Dka2ZQNd2SVw31q3hVTrCQ130_head.
- 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.