Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP821283.RAyu1f2phkKhP0rJqRwL1QScA5v1K1bl4UXkPo7fp25Rw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP821283.RAyu1f2phkKhP0rJqRwL1QScA5v1K1bl4UXkPo7fp25Rw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP821283.RAyu1f2phkKhP0rJqRwL1QScA5v1K1bl4UXkPo7fp25Rw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP821283.RAyu1f2phkKhP0rJqRwL1QScA5v1K1bl4UXkPo7fp25Rw130_provenance.
- NP821283.RAyu1f2phkKhP0rJqRwL1QScA5v1K1bl4UXkPo7fp25Rw130_assertion description "[Mutations in SOD1, ANG, VAPB, TARDBP and FUS genes have been identified in amyotrophic lateral sclerosis (ALS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP821283.RAyu1f2phkKhP0rJqRwL1QScA5v1K1bl4UXkPo7fp25Rw130_provenance.
- NP821283.RAyu1f2phkKhP0rJqRwL1QScA5v1K1bl4UXkPo7fp25Rw130_assertion evidence source_evidence_literature NP821283.RAyu1f2phkKhP0rJqRwL1QScA5v1K1bl4UXkPo7fp25Rw130_provenance.
- NP821283.RAyu1f2phkKhP0rJqRwL1QScA5v1K1bl4UXkPo7fp25Rw130_assertion SIO_000772 20577002 NP821283.RAyu1f2phkKhP0rJqRwL1QScA5v1K1bl4UXkPo7fp25Rw130_provenance.
- NP821283.RAyu1f2phkKhP0rJqRwL1QScA5v1K1bl4UXkPo7fp25Rw130_assertion wasDerivedFrom befree-2016 NP821283.RAyu1f2phkKhP0rJqRwL1QScA5v1K1bl4UXkPo7fp25Rw130_provenance.
- NP821283.RAyu1f2phkKhP0rJqRwL1QScA5v1K1bl4UXkPo7fp25Rw130_assertion wasGeneratedBy ECO_0000203 NP821283.RAyu1f2phkKhP0rJqRwL1QScA5v1K1bl4UXkPo7fp25Rw130_provenance.
- befree-2016 importedOn "2016-02-19" NP821283.RAyu1f2phkKhP0rJqRwL1QScA5v1K1bl4UXkPo7fp25Rw130_provenance.