Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP804086.RA_EEJE8mIQeGkNznR5TCAO4bZorND4pyE9g2ZpkhfMWc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP804086.RA_EEJE8mIQeGkNznR5TCAO4bZorND4pyE9g2ZpkhfMWc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP804086.RA_EEJE8mIQeGkNznR5TCAO4bZorND4pyE9g2ZpkhfMWc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP804086.RA_EEJE8mIQeGkNznR5TCAO4bZorND4pyE9g2ZpkhfMWc130_provenance.
- NP804086.RA_EEJE8mIQeGkNznR5TCAO4bZorND4pyE9g2ZpkhfMWc130_assertion description "[Mutations in SOD1 cause familial amyotrophic lateral sclerosis (ALS), whose pathologic features include mitochondrial bioenergetic dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP804086.RA_EEJE8mIQeGkNznR5TCAO4bZorND4pyE9g2ZpkhfMWc130_provenance.
- NP804086.RA_EEJE8mIQeGkNznR5TCAO4bZorND4pyE9g2ZpkhfMWc130_assertion evidence source_evidence_literature NP804086.RA_EEJE8mIQeGkNznR5TCAO4bZorND4pyE9g2ZpkhfMWc130_provenance.
- NP804086.RA_EEJE8mIQeGkNznR5TCAO4bZorND4pyE9g2ZpkhfMWc130_assertion SIO_000772 20367259 NP804086.RA_EEJE8mIQeGkNznR5TCAO4bZorND4pyE9g2ZpkhfMWc130_provenance.
- NP804086.RA_EEJE8mIQeGkNznR5TCAO4bZorND4pyE9g2ZpkhfMWc130_assertion wasDerivedFrom befree-2016 NP804086.RA_EEJE8mIQeGkNznR5TCAO4bZorND4pyE9g2ZpkhfMWc130_provenance.
- NP804086.RA_EEJE8mIQeGkNznR5TCAO4bZorND4pyE9g2ZpkhfMWc130_assertion wasGeneratedBy ECO_0000203 NP804086.RA_EEJE8mIQeGkNznR5TCAO4bZorND4pyE9g2ZpkhfMWc130_provenance.
- befree-2016 importedOn "2016-02-19" NP804086.RA_EEJE8mIQeGkNznR5TCAO4bZorND4pyE9g2ZpkhfMWc130_provenance.