Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP217605.RAYeHh5rUq_9S3-SBT-pHdyQrDNwCMzP4hGF-xLsZEjFU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP217605.RAYeHh5rUq_9S3-SBT-pHdyQrDNwCMzP4hGF-xLsZEjFU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP217605.RAYeHh5rUq_9S3-SBT-pHdyQrDNwCMzP4hGF-xLsZEjFU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP217605.RAYeHh5rUq_9S3-SBT-pHdyQrDNwCMzP4hGF-xLsZEjFU130_provenance.
- NP217605.RAYeHh5rUq_9S3-SBT-pHdyQrDNwCMzP4hGF-xLsZEjFU130_assertion description "[The mutant 128R allele of the E-selectin gene is associated with angiographic severe coronary artery disease (CAD) in Saudi Arabs/association is lost after adjustment for traditional CAD risk factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217605.RAYeHh5rUq_9S3-SBT-pHdyQrDNwCMzP4hGF-xLsZEjFU130_provenance.
- NP217605.RAYeHh5rUq_9S3-SBT-pHdyQrDNwCMzP4hGF-xLsZEjFU130_assertion evidence source_evidence_literature NP217605.RAYeHh5rUq_9S3-SBT-pHdyQrDNwCMzP4hGF-xLsZEjFU130_provenance.
- NP217605.RAYeHh5rUq_9S3-SBT-pHdyQrDNwCMzP4hGF-xLsZEjFU130_assertion SIO_000772 16756647 NP217605.RAYeHh5rUq_9S3-SBT-pHdyQrDNwCMzP4hGF-xLsZEjFU130_provenance.
- NP217605.RAYeHh5rUq_9S3-SBT-pHdyQrDNwCMzP4hGF-xLsZEjFU130_assertion wasDerivedFrom lhgdn-20090331 NP217605.RAYeHh5rUq_9S3-SBT-pHdyQrDNwCMzP4hGF-xLsZEjFU130_provenance.
- NP217605.RAYeHh5rUq_9S3-SBT-pHdyQrDNwCMzP4hGF-xLsZEjFU130_assertion wasGeneratedBy ECO_0000203 NP217605.RAYeHh5rUq_9S3-SBT-pHdyQrDNwCMzP4hGF-xLsZEjFU130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP217605.RAYeHh5rUq_9S3-SBT-pHdyQrDNwCMzP4hGF-xLsZEjFU130_provenance.