Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP713223.RAz540AbXDa2D5rtUcSr7vkQEkQvMejUHpx6VQg3RSxVA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP713223.RAz540AbXDa2D5rtUcSr7vkQEkQvMejUHpx6VQg3RSxVA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP713223.RAz540AbXDa2D5rtUcSr7vkQEkQvMejUHpx6VQg3RSxVA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP713223.RAz540AbXDa2D5rtUcSr7vkQEkQvMejUHpx6VQg3RSxVA130_provenance.
- NP713223.RAz540AbXDa2D5rtUcSr7vkQEkQvMejUHpx6VQg3RSxVA130_assertion description "[MRX87 patients had moderate to profound cognition impairment and a combination of minor congenital anomalies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP713223.RAz540AbXDa2D5rtUcSr7vkQEkQvMejUHpx6VQg3RSxVA130_provenance.
- NP713223.RAz540AbXDa2D5rtUcSr7vkQEkQvMejUHpx6VQg3RSxVA130_assertion evidence source_evidence_literature NP713223.RAz540AbXDa2D5rtUcSr7vkQEkQvMejUHpx6VQg3RSxVA130_provenance.
- NP713223.RAz540AbXDa2D5rtUcSr7vkQEkQvMejUHpx6VQg3RSxVA130_assertion SIO_000772 17480217 NP713223.RAz540AbXDa2D5rtUcSr7vkQEkQvMejUHpx6VQg3RSxVA130_provenance.
- NP713223.RAz540AbXDa2D5rtUcSr7vkQEkQvMejUHpx6VQg3RSxVA130_assertion wasDerivedFrom befree-20140225 NP713223.RAz540AbXDa2D5rtUcSr7vkQEkQvMejUHpx6VQg3RSxVA130_provenance.
- NP713223.RAz540AbXDa2D5rtUcSr7vkQEkQvMejUHpx6VQg3RSxVA130_assertion wasGeneratedBy ECO_0000203 NP713223.RAz540AbXDa2D5rtUcSr7vkQEkQvMejUHpx6VQg3RSxVA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP713223.RAz540AbXDa2D5rtUcSr7vkQEkQvMejUHpx6VQg3RSxVA130_provenance.