Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP167562.RA0RXcxB98FIOM2wup-9yD1bxlZBU9MToL_GdFhRlXWsI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP167562.RA0RXcxB98FIOM2wup-9yD1bxlZBU9MToL_GdFhRlXWsI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP167562.RA0RXcxB98FIOM2wup-9yD1bxlZBU9MToL_GdFhRlXWsI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP167562.RA0RXcxB98FIOM2wup-9yD1bxlZBU9MToL_GdFhRlXWsI130_provenance.
- NP167562.RA0RXcxB98FIOM2wup-9yD1bxlZBU9MToL_GdFhRlXWsI130_assertion description "[Our results indicated a strong association of sequence variants of HMGCR, SREBF1 and ABCG8 genes with the reduction of LDL-C after statin treatment in a Chinese population. Future studies on the genes of drug-metabolism enzymes and transporters are warran]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP167562.RA0RXcxB98FIOM2wup-9yD1bxlZBU9MToL_GdFhRlXWsI130_provenance.
- NP167562.RA0RXcxB98FIOM2wup-9yD1bxlZBU9MToL_GdFhRlXWsI130_assertion evidence source_evidence_literature NP167562.RA0RXcxB98FIOM2wup-9yD1bxlZBU9MToL_GdFhRlXWsI130_provenance.
- NP167562.RA0RXcxB98FIOM2wup-9yD1bxlZBU9MToL_GdFhRlXWsI130_assertion SIO_000772 20235787 NP167562.RA0RXcxB98FIOM2wup-9yD1bxlZBU9MToL_GdFhRlXWsI130_provenance.
- NP167562.RA0RXcxB98FIOM2wup-9yD1bxlZBU9MToL_GdFhRlXWsI130_assertion wasDerivedFrom gad-20150221 NP167562.RA0RXcxB98FIOM2wup-9yD1bxlZBU9MToL_GdFhRlXWsI130_provenance.
- NP167562.RA0RXcxB98FIOM2wup-9yD1bxlZBU9MToL_GdFhRlXWsI130_assertion wasGeneratedBy ECO_0000203 NP167562.RA0RXcxB98FIOM2wup-9yD1bxlZBU9MToL_GdFhRlXWsI130_provenance.
- gad-20150221 importedOn "2015-02-21" NP167562.RA0RXcxB98FIOM2wup-9yD1bxlZBU9MToL_GdFhRlXWsI130_provenance.