Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP854043.RAncIoCSX4lqQnyhykKlCgTMQTCO59LEveFemJOArultw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP854043.RAncIoCSX4lqQnyhykKlCgTMQTCO59LEveFemJOArultw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP854043.RAncIoCSX4lqQnyhykKlCgTMQTCO59LEveFemJOArultw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP854043.RAncIoCSX4lqQnyhykKlCgTMQTCO59LEveFemJOArultw130_provenance.
- NP854043.RAncIoCSX4lqQnyhykKlCgTMQTCO59LEveFemJOArultw130_assertion wasGeneratedBy ECO_0000203 NP854043.RAncIoCSX4lqQnyhykKlCgTMQTCO59LEveFemJOArultw130_provenance.
- NP854043.RAncIoCSX4lqQnyhykKlCgTMQTCO59LEveFemJOArultw130_assertion wasDerivedFrom befree-20140225 NP854043.RAncIoCSX4lqQnyhykKlCgTMQTCO59LEveFemJOArultw130_provenance.
- NP854043.RAncIoCSX4lqQnyhykKlCgTMQTCO59LEveFemJOArultw130_assertion SIO_000772 23545315 NP854043.RAncIoCSX4lqQnyhykKlCgTMQTCO59LEveFemJOArultw130_provenance.
- NP854043.RAncIoCSX4lqQnyhykKlCgTMQTCO59LEveFemJOArultw130_assertion evidence source_evidence_literature NP854043.RAncIoCSX4lqQnyhykKlCgTMQTCO59LEveFemJOArultw130_provenance.
- NP854043.RAncIoCSX4lqQnyhykKlCgTMQTCO59LEveFemJOArultw130_assertion description "[The allelic or genotypic frequencies of the rs699947 (5' untranslated regions, 5'UTR) and rs2010963 (5'UTR) polymorphisms in the CAD patients were significantly different from those in the healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP854043.RAncIoCSX4lqQnyhykKlCgTMQTCO59LEveFemJOArultw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP854043.RAncIoCSX4lqQnyhykKlCgTMQTCO59LEveFemJOArultw130_provenance.