Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP189363.RAFDEkWSI4LKyYVSy7RyKTqHCvt0ahtEgP5kWz5i_EoDI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP189363.RAFDEkWSI4LKyYVSy7RyKTqHCvt0ahtEgP5kWz5i_EoDI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP189363.RAFDEkWSI4LKyYVSy7RyKTqHCvt0ahtEgP5kWz5i_EoDI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP189363.RAFDEkWSI4LKyYVSy7RyKTqHCvt0ahtEgP5kWz5i_EoDI130_provenance.
- NP189363.RAFDEkWSI4LKyYVSy7RyKTqHCvt0ahtEgP5kWz5i_EoDI130_assertion description "[Genotypes for ABCA1, IRAK1, and ROS1 may prove useful for assessment of the genetic risk for atherothrombotic cerebral infarction, whereas those for LIMK1 and CYP3A4 may be similarly beneficial in assessment of the genetic risk for intracerebral hemorrhage and subarachnoid hemorrhage, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP189363.RAFDEkWSI4LKyYVSy7RyKTqHCvt0ahtEgP5kWz5i_EoDI130_provenance.
- NP189363.RAFDEkWSI4LKyYVSy7RyKTqHCvt0ahtEgP5kWz5i_EoDI130_assertion evidence source_evidence_literature NP189363.RAFDEkWSI4LKyYVSy7RyKTqHCvt0ahtEgP5kWz5i_EoDI130_provenance.
- NP189363.RAFDEkWSI4LKyYVSy7RyKTqHCvt0ahtEgP5kWz5i_EoDI130_assertion SIO_000772 18566305 NP189363.RAFDEkWSI4LKyYVSy7RyKTqHCvt0ahtEgP5kWz5i_EoDI130_provenance.
- NP189363.RAFDEkWSI4LKyYVSy7RyKTqHCvt0ahtEgP5kWz5i_EoDI130_assertion wasDerivedFrom befree-20140225 NP189363.RAFDEkWSI4LKyYVSy7RyKTqHCvt0ahtEgP5kWz5i_EoDI130_provenance.
- NP189363.RAFDEkWSI4LKyYVSy7RyKTqHCvt0ahtEgP5kWz5i_EoDI130_assertion wasGeneratedBy ECO_0000203 NP189363.RAFDEkWSI4LKyYVSy7RyKTqHCvt0ahtEgP5kWz5i_EoDI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP189363.RAFDEkWSI4LKyYVSy7RyKTqHCvt0ahtEgP5kWz5i_EoDI130_provenance.