Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP913398.RAO_omSYMm2lOxTH6-AVohsfuRsavksDintXlIp2AXQ0c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP913398.RAO_omSYMm2lOxTH6-AVohsfuRsavksDintXlIp2AXQ0c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP913398.RAO_omSYMm2lOxTH6-AVohsfuRsavksDintXlIp2AXQ0c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP913398.RAO_omSYMm2lOxTH6-AVohsfuRsavksDintXlIp2AXQ0c130_provenance.
- NP913398.RAO_omSYMm2lOxTH6-AVohsfuRsavksDintXlIp2AXQ0c130_assertion description "[Allele and genotype frequencies of a promoter single nucleotide polymorphism (SNP) in ACT gene were investigated in patients with benign prostate hypertrophy (BHP) or PCa and controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP913398.RAO_omSYMm2lOxTH6-AVohsfuRsavksDintXlIp2AXQ0c130_provenance.
- NP913398.RAO_omSYMm2lOxTH6-AVohsfuRsavksDintXlIp2AXQ0c130_assertion evidence source_evidence_literature NP913398.RAO_omSYMm2lOxTH6-AVohsfuRsavksDintXlIp2AXQ0c130_provenance.
- NP913398.RAO_omSYMm2lOxTH6-AVohsfuRsavksDintXlIp2AXQ0c130_assertion SIO_000772 18383875 NP913398.RAO_omSYMm2lOxTH6-AVohsfuRsavksDintXlIp2AXQ0c130_provenance.
- NP913398.RAO_omSYMm2lOxTH6-AVohsfuRsavksDintXlIp2AXQ0c130_assertion wasDerivedFrom befree-20140225 NP913398.RAO_omSYMm2lOxTH6-AVohsfuRsavksDintXlIp2AXQ0c130_provenance.
- NP913398.RAO_omSYMm2lOxTH6-AVohsfuRsavksDintXlIp2AXQ0c130_assertion wasGeneratedBy ECO_0000203 NP913398.RAO_omSYMm2lOxTH6-AVohsfuRsavksDintXlIp2AXQ0c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP913398.RAO_omSYMm2lOxTH6-AVohsfuRsavksDintXlIp2AXQ0c130_provenance.