Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1102251.RAJZr1Q1H3Y7icMmwJDgROx0OzxIhbvI2hXNz-F6FSzko130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1102251.RAJZr1Q1H3Y7icMmwJDgROx0OzxIhbvI2hXNz-F6FSzko130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1102251.RAJZr1Q1H3Y7icMmwJDgROx0OzxIhbvI2hXNz-F6FSzko130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1102251.RAJZr1Q1H3Y7icMmwJDgROx0OzxIhbvI2hXNz-F6FSzko130_provenance.
- befree-2016 importedOn "2016-02-19" NP1102251.RAJZr1Q1H3Y7icMmwJDgROx0OzxIhbvI2hXNz-F6FSzko130_provenance.
- NP1102251.RAJZr1Q1H3Y7icMmwJDgROx0OzxIhbvI2hXNz-F6FSzko130_assertion wasGeneratedBy ECO_0000203 NP1102251.RAJZr1Q1H3Y7icMmwJDgROx0OzxIhbvI2hXNz-F6FSzko130_provenance.
- NP1102251.RAJZr1Q1H3Y7icMmwJDgROx0OzxIhbvI2hXNz-F6FSzko130_assertion wasDerivedFrom befree-2016 NP1102251.RAJZr1Q1H3Y7icMmwJDgROx0OzxIhbvI2hXNz-F6FSzko130_provenance.
- NP1102251.RAJZr1Q1H3Y7icMmwJDgROx0OzxIhbvI2hXNz-F6FSzko130_assertion SIO_000772 23942138 NP1102251.RAJZr1Q1H3Y7icMmwJDgROx0OzxIhbvI2hXNz-F6FSzko130_provenance.
- NP1102251.RAJZr1Q1H3Y7icMmwJDgROx0OzxIhbvI2hXNz-F6FSzko130_assertion evidence source_evidence_literature NP1102251.RAJZr1Q1H3Y7icMmwJDgROx0OzxIhbvI2hXNz-F6FSzko130_provenance.
- NP1102251.RAJZr1Q1H3Y7icMmwJDgROx0OzxIhbvI2hXNz-F6FSzko130_assertion description "[SLCO1B1 genetic variant associated with statin-induced myopathy: a proof-of-concept study using the clinical practice research datalink.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1102251.RAJZr1Q1H3Y7icMmwJDgROx0OzxIhbvI2hXNz-F6FSzko130_provenance.