Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP54687.RAzvMWrpdzyPDRPVxN0S93znFQvZ0Uzvc0V0M-PMHuOC8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP54687.RAzvMWrpdzyPDRPVxN0S93znFQvZ0Uzvc0V0M-PMHuOC8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP54687.RAzvMWrpdzyPDRPVxN0S93znFQvZ0Uzvc0V0M-PMHuOC8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP54687.RAzvMWrpdzyPDRPVxN0S93znFQvZ0Uzvc0V0M-PMHuOC8130_provenance.
- NP54687.RAzvMWrpdzyPDRPVxN0S93znFQvZ0Uzvc0V0M-PMHuOC8130_assertion description "[In conclusion, 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." NP54687.RAzvMWrpdzyPDRPVxN0S93znFQvZ0Uzvc0V0M-PMHuOC8130_provenance.
- NP54687.RAzvMWrpdzyPDRPVxN0S93znFQvZ0Uzvc0V0M-PMHuOC8130_assertion evidence source_evidence_literature NP54687.RAzvMWrpdzyPDRPVxN0S93znFQvZ0Uzvc0V0M-PMHuOC8130_provenance.
- NP54687.RAzvMWrpdzyPDRPVxN0S93znFQvZ0Uzvc0V0M-PMHuOC8130_assertion SIO_000772 17641958 NP54687.RAzvMWrpdzyPDRPVxN0S93znFQvZ0Uzvc0V0M-PMHuOC8130_provenance.
- NP54687.RAzvMWrpdzyPDRPVxN0S93znFQvZ0Uzvc0V0M-PMHuOC8130_assertion wasDerivedFrom gad-20150221 NP54687.RAzvMWrpdzyPDRPVxN0S93znFQvZ0Uzvc0V0M-PMHuOC8130_provenance.
- NP54687.RAzvMWrpdzyPDRPVxN0S93znFQvZ0Uzvc0V0M-PMHuOC8130_assertion wasGeneratedBy ECO_0000203 NP54687.RAzvMWrpdzyPDRPVxN0S93znFQvZ0Uzvc0V0M-PMHuOC8130_provenance.
- gad-20150221 importedOn "2015-02-21" NP54687.RAzvMWrpdzyPDRPVxN0S93znFQvZ0Uzvc0V0M-PMHuOC8130_provenance.