Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP465886.RAEfOijgyt1m1Tpg1ECbWonxpSzKLTLJulGC8MWZrdsqQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP465886.RAEfOijgyt1m1Tpg1ECbWonxpSzKLTLJulGC8MWZrdsqQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP465886.RAEfOijgyt1m1Tpg1ECbWonxpSzKLTLJulGC8MWZrdsqQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP465886.RAEfOijgyt1m1Tpg1ECbWonxpSzKLTLJulGC8MWZrdsqQ130_provenance.
- NP465886.RAEfOijgyt1m1Tpg1ECbWonxpSzKLTLJulGC8MWZrdsqQ130_assertion description "[SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP465886.RAEfOijgyt1m1Tpg1ECbWonxpSzKLTLJulGC8MWZrdsqQ130_provenance.
- NP465886.RAEfOijgyt1m1Tpg1ECbWonxpSzKLTLJulGC8MWZrdsqQ130_assertion evidence source_evidence_literature NP465886.RAEfOijgyt1m1Tpg1ECbWonxpSzKLTLJulGC8MWZrdsqQ130_provenance.
- NP465886.RAEfOijgyt1m1Tpg1ECbWonxpSzKLTLJulGC8MWZrdsqQ130_assertion SIO_000772 20577002 NP465886.RAEfOijgyt1m1Tpg1ECbWonxpSzKLTLJulGC8MWZrdsqQ130_provenance.
- NP465886.RAEfOijgyt1m1Tpg1ECbWonxpSzKLTLJulGC8MWZrdsqQ130_assertion wasDerivedFrom befree-20140225 NP465886.RAEfOijgyt1m1Tpg1ECbWonxpSzKLTLJulGC8MWZrdsqQ130_provenance.
- NP465886.RAEfOijgyt1m1Tpg1ECbWonxpSzKLTLJulGC8MWZrdsqQ130_assertion wasGeneratedBy ECO_0000203 NP465886.RAEfOijgyt1m1Tpg1ECbWonxpSzKLTLJulGC8MWZrdsqQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP465886.RAEfOijgyt1m1Tpg1ECbWonxpSzKLTLJulGC8MWZrdsqQ130_provenance.