Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP896898.RAAZVVnT7Dxj62PBUDi97zWz3dJd6KRSENpp5aWoTPYeo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP896898.RAAZVVnT7Dxj62PBUDi97zWz3dJd6KRSENpp5aWoTPYeo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP896898.RAAZVVnT7Dxj62PBUDi97zWz3dJd6KRSENpp5aWoTPYeo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP896898.RAAZVVnT7Dxj62PBUDi97zWz3dJd6KRSENpp5aWoTPYeo130_provenance.
- NP896898.RAAZVVnT7Dxj62PBUDi97zWz3dJd6KRSENpp5aWoTPYeo130_assertion description "[It has been demonstrated that the SNPs associated with increased risk of human diseases such as ?-, ?- and ?-thalassemia, myocardial infarction and thrombophlebitis, changes in immune response, amyotrophic lateral sclerosis, lung cancer and hemophilia B Leyden cause 2-4-fold changes in TBP/TATA affinity in most cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP896898.RAAZVVnT7Dxj62PBUDi97zWz3dJd6KRSENpp5aWoTPYeo130_provenance.
- NP896898.RAAZVVnT7Dxj62PBUDi97zWz3dJd6KRSENpp5aWoTPYeo130_assertion evidence source_evidence_literature NP896898.RAAZVVnT7Dxj62PBUDi97zWz3dJd6KRSENpp5aWoTPYeo130_provenance.
- NP896898.RAAZVVnT7Dxj62PBUDi97zWz3dJd6KRSENpp5aWoTPYeo130_assertion SIO_000772 23424617 NP896898.RAAZVVnT7Dxj62PBUDi97zWz3dJd6KRSENpp5aWoTPYeo130_provenance.
- NP896898.RAAZVVnT7Dxj62PBUDi97zWz3dJd6KRSENpp5aWoTPYeo130_assertion wasDerivedFrom befree-20140225 NP896898.RAAZVVnT7Dxj62PBUDi97zWz3dJd6KRSENpp5aWoTPYeo130_provenance.
- NP896898.RAAZVVnT7Dxj62PBUDi97zWz3dJd6KRSENpp5aWoTPYeo130_assertion wasGeneratedBy ECO_0000203 NP896898.RAAZVVnT7Dxj62PBUDi97zWz3dJd6KRSENpp5aWoTPYeo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP896898.RAAZVVnT7Dxj62PBUDi97zWz3dJd6KRSENpp5aWoTPYeo130_provenance.