Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP817675.RAUU9JTbiRhs3gU6A4H4RpGWFklRIDf2_dnrcMr5Emsxk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP817675.RAUU9JTbiRhs3gU6A4H4RpGWFklRIDf2_dnrcMr5Emsxk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP817675.RAUU9JTbiRhs3gU6A4H4RpGWFklRIDf2_dnrcMr5Emsxk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP817675.RAUU9JTbiRhs3gU6A4H4RpGWFklRIDf2_dnrcMr5Emsxk130_provenance.
- NP817675.RAUU9JTbiRhs3gU6A4H4RpGWFklRIDf2_dnrcMr5Emsxk130_assertion description "[ALS2 is a causative gene for a juvenile autosomal recessive form of motor neuron diseases (MNDs), including amyotrophic lateral sclerosis 2 (ALS2), juvenile primary lateral sclerosis, and infantile-onset ascending hereditary spastic paralysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP817675.RAUU9JTbiRhs3gU6A4H4RpGWFklRIDf2_dnrcMr5Emsxk130_provenance.
- NP817675.RAUU9JTbiRhs3gU6A4H4RpGWFklRIDf2_dnrcMr5Emsxk130_assertion evidence source_evidence_literature NP817675.RAUU9JTbiRhs3gU6A4H4RpGWFklRIDf2_dnrcMr5Emsxk130_provenance.
- NP817675.RAUU9JTbiRhs3gU6A4H4RpGWFklRIDf2_dnrcMr5Emsxk130_assertion SIO_000772 17566607 NP817675.RAUU9JTbiRhs3gU6A4H4RpGWFklRIDf2_dnrcMr5Emsxk130_provenance.
- NP817675.RAUU9JTbiRhs3gU6A4H4RpGWFklRIDf2_dnrcMr5Emsxk130_assertion wasDerivedFrom befree-20140225 NP817675.RAUU9JTbiRhs3gU6A4H4RpGWFklRIDf2_dnrcMr5Emsxk130_provenance.
- NP817675.RAUU9JTbiRhs3gU6A4H4RpGWFklRIDf2_dnrcMr5Emsxk130_assertion wasGeneratedBy ECO_0000203 NP817675.RAUU9JTbiRhs3gU6A4H4RpGWFklRIDf2_dnrcMr5Emsxk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP817675.RAUU9JTbiRhs3gU6A4H4RpGWFklRIDf2_dnrcMr5Emsxk130_provenance.