Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP124903.RApZ6F9UbXS0BfP2HNJ2fyICgXm0JJ_Fogkks-wt6aLME130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP124903.RApZ6F9UbXS0BfP2HNJ2fyICgXm0JJ_Fogkks-wt6aLME130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP124903.RApZ6F9UbXS0BfP2HNJ2fyICgXm0JJ_Fogkks-wt6aLME130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP124903.RApZ6F9UbXS0BfP2HNJ2fyICgXm0JJ_Fogkks-wt6aLME130_provenance.
- NP124903.RApZ6F9UbXS0BfP2HNJ2fyICgXm0JJ_Fogkks-wt6aLME130_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 hemorrhag]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP124903.RApZ6F9UbXS0BfP2HNJ2fyICgXm0JJ_Fogkks-wt6aLME130_provenance.
- NP124903.RApZ6F9UbXS0BfP2HNJ2fyICgXm0JJ_Fogkks-wt6aLME130_assertion evidence source_evidence_literature NP124903.RApZ6F9UbXS0BfP2HNJ2fyICgXm0JJ_Fogkks-wt6aLME130_provenance.
- NP124903.RApZ6F9UbXS0BfP2HNJ2fyICgXm0JJ_Fogkks-wt6aLME130_assertion SIO_000772 18566305 NP124903.RApZ6F9UbXS0BfP2HNJ2fyICgXm0JJ_Fogkks-wt6aLME130_provenance.
- NP124903.RApZ6F9UbXS0BfP2HNJ2fyICgXm0JJ_Fogkks-wt6aLME130_assertion wasDerivedFrom gad-20150221 NP124903.RApZ6F9UbXS0BfP2HNJ2fyICgXm0JJ_Fogkks-wt6aLME130_provenance.
- NP124903.RApZ6F9UbXS0BfP2HNJ2fyICgXm0JJ_Fogkks-wt6aLME130_assertion wasGeneratedBy ECO_0000203 NP124903.RApZ6F9UbXS0BfP2HNJ2fyICgXm0JJ_Fogkks-wt6aLME130_provenance.
- gad-20150221 importedOn "2015-02-21" NP124903.RApZ6F9UbXS0BfP2HNJ2fyICgXm0JJ_Fogkks-wt6aLME130_provenance.