Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP206447.RAOqjyQg6n2zTkJhcUvZ3Fq7lVM3QEiFz6CtgkbxJvJsE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP206447.RAOqjyQg6n2zTkJhcUvZ3Fq7lVM3QEiFz6CtgkbxJvJsE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP206447.RAOqjyQg6n2zTkJhcUvZ3Fq7lVM3QEiFz6CtgkbxJvJsE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP206447.RAOqjyQg6n2zTkJhcUvZ3Fq7lVM3QEiFz6CtgkbxJvJsE130_provenance.
- NP206447.RAOqjyQg6n2zTkJhcUvZ3Fq7lVM3QEiFz6CtgkbxJvJsE130_assertion description "[The C3435T MDR1 polymorphism may involve susceptibility to & the clinical outcome of childhood ALL/of the TT genotype are more at risk of developing ALL than others, whereas CC genotype carriers are supposed to have worse prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206447.RAOqjyQg6n2zTkJhcUvZ3Fq7lVM3QEiFz6CtgkbxJvJsE130_provenance.
- NP206447.RAOqjyQg6n2zTkJhcUvZ3Fq7lVM3QEiFz6CtgkbxJvJsE130_assertion evidence source_evidence_literature NP206447.RAOqjyQg6n2zTkJhcUvZ3Fq7lVM3QEiFz6CtgkbxJvJsE130_provenance.
- NP206447.RAOqjyQg6n2zTkJhcUvZ3Fq7lVM3QEiFz6CtgkbxJvJsE130_assertion SIO_000772 15059065 NP206447.RAOqjyQg6n2zTkJhcUvZ3Fq7lVM3QEiFz6CtgkbxJvJsE130_provenance.
- NP206447.RAOqjyQg6n2zTkJhcUvZ3Fq7lVM3QEiFz6CtgkbxJvJsE130_assertion wasDerivedFrom lhgdn-20090331 NP206447.RAOqjyQg6n2zTkJhcUvZ3Fq7lVM3QEiFz6CtgkbxJvJsE130_provenance.
- NP206447.RAOqjyQg6n2zTkJhcUvZ3Fq7lVM3QEiFz6CtgkbxJvJsE130_assertion wasGeneratedBy ECO_0000203 NP206447.RAOqjyQg6n2zTkJhcUvZ3Fq7lVM3QEiFz6CtgkbxJvJsE130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP206447.RAOqjyQg6n2zTkJhcUvZ3Fq7lVM3QEiFz6CtgkbxJvJsE130_provenance.