Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP864056.RA99tSsJfX8wOyN0ZGmoggdcTtVWD5nFlx8rPJzIo9VYA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP864056.RA99tSsJfX8wOyN0ZGmoggdcTtVWD5nFlx8rPJzIo9VYA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP864056.RA99tSsJfX8wOyN0ZGmoggdcTtVWD5nFlx8rPJzIo9VYA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP864056.RA99tSsJfX8wOyN0ZGmoggdcTtVWD5nFlx8rPJzIo9VYA130_provenance.
- NP864056.RA99tSsJfX8wOyN0ZGmoggdcTtVWD5nFlx8rPJzIo9VYA130_assertion description "[Interestingly, a 6-fold increased frequency of the homozygous variant genotype was observed among patients with isolated trisomy 8 (p<0.0001), suggesting that null NQO1 activity may influence the occurrence of +8 in MDS/AML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP864056.RA99tSsJfX8wOyN0ZGmoggdcTtVWD5nFlx8rPJzIo9VYA130_provenance.
- NP864056.RA99tSsJfX8wOyN0ZGmoggdcTtVWD5nFlx8rPJzIo9VYA130_assertion evidence source_evidence_literature NP864056.RA99tSsJfX8wOyN0ZGmoggdcTtVWD5nFlx8rPJzIo9VYA130_provenance.
- NP864056.RA99tSsJfX8wOyN0ZGmoggdcTtVWD5nFlx8rPJzIo9VYA130_assertion SIO_000772 23643325 NP864056.RA99tSsJfX8wOyN0ZGmoggdcTtVWD5nFlx8rPJzIo9VYA130_provenance.
- NP864056.RA99tSsJfX8wOyN0ZGmoggdcTtVWD5nFlx8rPJzIo9VYA130_assertion wasDerivedFrom befree-20140225 NP864056.RA99tSsJfX8wOyN0ZGmoggdcTtVWD5nFlx8rPJzIo9VYA130_provenance.
- NP864056.RA99tSsJfX8wOyN0ZGmoggdcTtVWD5nFlx8rPJzIo9VYA130_assertion wasGeneratedBy ECO_0000203 NP864056.RA99tSsJfX8wOyN0ZGmoggdcTtVWD5nFlx8rPJzIo9VYA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP864056.RA99tSsJfX8wOyN0ZGmoggdcTtVWD5nFlx8rPJzIo9VYA130_provenance.