Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP756629.RAumWv9iwUX1D5gLbCGNvP9IBtzqA0M0E1nh2eq_9t_CQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP756629.RAumWv9iwUX1D5gLbCGNvP9IBtzqA0M0E1nh2eq_9t_CQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP756629.RAumWv9iwUX1D5gLbCGNvP9IBtzqA0M0E1nh2eq_9t_CQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP756629.RAumWv9iwUX1D5gLbCGNvP9IBtzqA0M0E1nh2eq_9t_CQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP756629.RAumWv9iwUX1D5gLbCGNvP9IBtzqA0M0E1nh2eq_9t_CQ130_provenance.
- NP756629.RAumWv9iwUX1D5gLbCGNvP9IBtzqA0M0E1nh2eq_9t_CQ130_assertion wasGeneratedBy ECO_0000203 NP756629.RAumWv9iwUX1D5gLbCGNvP9IBtzqA0M0E1nh2eq_9t_CQ130_provenance.
- NP756629.RAumWv9iwUX1D5gLbCGNvP9IBtzqA0M0E1nh2eq_9t_CQ130_assertion wasDerivedFrom befree-2016 NP756629.RAumWv9iwUX1D5gLbCGNvP9IBtzqA0M0E1nh2eq_9t_CQ130_provenance.
- NP756629.RAumWv9iwUX1D5gLbCGNvP9IBtzqA0M0E1nh2eq_9t_CQ130_assertion SIO_000772 19669651 NP756629.RAumWv9iwUX1D5gLbCGNvP9IBtzqA0M0E1nh2eq_9t_CQ130_provenance.
- NP756629.RAumWv9iwUX1D5gLbCGNvP9IBtzqA0M0E1nh2eq_9t_CQ130_assertion evidence source_evidence_literature NP756629.RAumWv9iwUX1D5gLbCGNvP9IBtzqA0M0E1nh2eq_9t_CQ130_provenance.
- NP756629.RAumWv9iwUX1D5gLbCGNvP9IBtzqA0M0E1nh2eq_9t_CQ130_assertion description "[Mutations in the gene encoding the fused in sarcoma (FUS) protein have recently been identified as a cause of familial amyotrophic lateral sclerosis (ALS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP756629.RAumWv9iwUX1D5gLbCGNvP9IBtzqA0M0E1nh2eq_9t_CQ130_provenance.