Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP500148.RArtbewU640mDjVD89Dx7gGMEybpfmFtLTc0DfU6XH-rg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP500148.RArtbewU640mDjVD89Dx7gGMEybpfmFtLTc0DfU6XH-rg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP500148.RArtbewU640mDjVD89Dx7gGMEybpfmFtLTc0DfU6XH-rg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP500148.RArtbewU640mDjVD89Dx7gGMEybpfmFtLTc0DfU6XH-rg130_provenance.
- NP500148.RArtbewU640mDjVD89Dx7gGMEybpfmFtLTc0DfU6XH-rg130_assertion description "[The most frequent genetic causes of amyotrophic lateral sclerosis (ALS) determined so far are mutations occurring in the gene coding for copper/zinc superoxide dismutase (Cu,Zn-SOD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP500148.RArtbewU640mDjVD89Dx7gGMEybpfmFtLTc0DfU6XH-rg130_provenance.
- NP500148.RArtbewU640mDjVD89Dx7gGMEybpfmFtLTc0DfU6XH-rg130_assertion evidence source_evidence_literature NP500148.RArtbewU640mDjVD89Dx7gGMEybpfmFtLTc0DfU6XH-rg130_provenance.
- NP500148.RArtbewU640mDjVD89Dx7gGMEybpfmFtLTc0DfU6XH-rg130_assertion SIO_000772 15965076 NP500148.RArtbewU640mDjVD89Dx7gGMEybpfmFtLTc0DfU6XH-rg130_provenance.
- NP500148.RArtbewU640mDjVD89Dx7gGMEybpfmFtLTc0DfU6XH-rg130_assertion wasDerivedFrom befree-2016 NP500148.RArtbewU640mDjVD89Dx7gGMEybpfmFtLTc0DfU6XH-rg130_provenance.
- NP500148.RArtbewU640mDjVD89Dx7gGMEybpfmFtLTc0DfU6XH-rg130_assertion wasGeneratedBy ECO_0000203 NP500148.RArtbewU640mDjVD89Dx7gGMEybpfmFtLTc0DfU6XH-rg130_provenance.
- befree-2016 importedOn "2016-02-19" NP500148.RArtbewU640mDjVD89Dx7gGMEybpfmFtLTc0DfU6XH-rg130_provenance.