Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP150769.RATGIp9Tam_rBOMdtCPH7LuEFquT1LIADcbb2W7FWUG2o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP150769.RATGIp9Tam_rBOMdtCPH7LuEFquT1LIADcbb2W7FWUG2o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP150769.RATGIp9Tam_rBOMdtCPH7LuEFquT1LIADcbb2W7FWUG2o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP150769.RATGIp9Tam_rBOMdtCPH7LuEFquT1LIADcbb2W7FWUG2o130_provenance.
- NP150769.RATGIp9Tam_rBOMdtCPH7LuEFquT1LIADcbb2W7FWUG2o130_assertion description "[, the CysLTR1 polymorphism may contribute to develop to the AIA phenotype and be used as a genetic marker for differentiating two major aspirin hypersensitivity phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150769.RATGIp9Tam_rBOMdtCPH7LuEFquT1LIADcbb2W7FWUG2o130_provenance.
- NP150769.RATGIp9Tam_rBOMdtCPH7LuEFquT1LIADcbb2W7FWUG2o130_assertion evidence source_evidence_literature NP150769.RATGIp9Tam_rBOMdtCPH7LuEFquT1LIADcbb2W7FWUG2o130_provenance.
- NP150769.RATGIp9Tam_rBOMdtCPH7LuEFquT1LIADcbb2W7FWUG2o130_assertion SIO_000772 17641958 NP150769.RATGIp9Tam_rBOMdtCPH7LuEFquT1LIADcbb2W7FWUG2o130_provenance.
- NP150769.RATGIp9Tam_rBOMdtCPH7LuEFquT1LIADcbb2W7FWUG2o130_assertion wasDerivedFrom gad-20150221 NP150769.RATGIp9Tam_rBOMdtCPH7LuEFquT1LIADcbb2W7FWUG2o130_provenance.
- NP150769.RATGIp9Tam_rBOMdtCPH7LuEFquT1LIADcbb2W7FWUG2o130_assertion wasGeneratedBy ECO_0000203 NP150769.RATGIp9Tam_rBOMdtCPH7LuEFquT1LIADcbb2W7FWUG2o130_provenance.
- gad-20150221 importedOn "2015-02-21" NP150769.RATGIp9Tam_rBOMdtCPH7LuEFquT1LIADcbb2W7FWUG2o130_provenance.