Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP897102.RABI8iaGnOrta7-74LIfOVk6egCnVbIyNHMffHwVwgsCk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP897102.RABI8iaGnOrta7-74LIfOVk6egCnVbIyNHMffHwVwgsCk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP897102.RABI8iaGnOrta7-74LIfOVk6egCnVbIyNHMffHwVwgsCk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP897102.RABI8iaGnOrta7-74LIfOVk6egCnVbIyNHMffHwVwgsCk130_provenance.
- NP897102.RABI8iaGnOrta7-74LIfOVk6egCnVbIyNHMffHwVwgsCk130_assertion description "[Moreover, the frequency of endothelin-1 Lys198Asn polymorphism was investigated with respect to the prevalence of several actual or historical endorgan damages (renal disorder, coronary artery disease, vascular events, vascular damage, and congestive heart failure) in hypertensive patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP897102.RABI8iaGnOrta7-74LIfOVk6egCnVbIyNHMffHwVwgsCk130_provenance.
- NP897102.RABI8iaGnOrta7-74LIfOVk6egCnVbIyNHMffHwVwgsCk130_assertion evidence source_evidence_literature NP897102.RABI8iaGnOrta7-74LIfOVk6egCnVbIyNHMffHwVwgsCk130_provenance.
- NP897102.RABI8iaGnOrta7-74LIfOVk6egCnVbIyNHMffHwVwgsCk130_assertion SIO_000772 18923236 NP897102.RABI8iaGnOrta7-74LIfOVk6egCnVbIyNHMffHwVwgsCk130_provenance.
- NP897102.RABI8iaGnOrta7-74LIfOVk6egCnVbIyNHMffHwVwgsCk130_assertion wasDerivedFrom befree-20140225 NP897102.RABI8iaGnOrta7-74LIfOVk6egCnVbIyNHMffHwVwgsCk130_provenance.
- NP897102.RABI8iaGnOrta7-74LIfOVk6egCnVbIyNHMffHwVwgsCk130_assertion wasGeneratedBy ECO_0000203 NP897102.RABI8iaGnOrta7-74LIfOVk6egCnVbIyNHMffHwVwgsCk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP897102.RABI8iaGnOrta7-74LIfOVk6egCnVbIyNHMffHwVwgsCk130_provenance.