Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP80396.RAip9pKCyVcRtK17Y9zXwvFeN_XK2MnvcFQJXMiDsaw90130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP80396.RAip9pKCyVcRtK17Y9zXwvFeN_XK2MnvcFQJXMiDsaw90130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP80396.RAip9pKCyVcRtK17Y9zXwvFeN_XK2MnvcFQJXMiDsaw90130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP80396.RAip9pKCyVcRtK17Y9zXwvFeN_XK2MnvcFQJXMiDsaw90130_provenance.
- NP80396.RAip9pKCyVcRtK17Y9zXwvFeN_XK2MnvcFQJXMiDsaw90130_assertion description "[The homozygous frequency of GSTP1 genotype did not differ significantly between groups of ALL (3.7%), ANLL patients (9.1%) and controls (4.9%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80396.RAip9pKCyVcRtK17Y9zXwvFeN_XK2MnvcFQJXMiDsaw90130_provenance.
- NP80396.RAip9pKCyVcRtK17Y9zXwvFeN_XK2MnvcFQJXMiDsaw90130_assertion evidence source_evidence_literature NP80396.RAip9pKCyVcRtK17Y9zXwvFeN_XK2MnvcFQJXMiDsaw90130_provenance.
- NP80396.RAip9pKCyVcRtK17Y9zXwvFeN_XK2MnvcFQJXMiDsaw90130_assertion SIO_000772 12827651 NP80396.RAip9pKCyVcRtK17Y9zXwvFeN_XK2MnvcFQJXMiDsaw90130_provenance.
- NP80396.RAip9pKCyVcRtK17Y9zXwvFeN_XK2MnvcFQJXMiDsaw90130_assertion wasDerivedFrom gad-20150221 NP80396.RAip9pKCyVcRtK17Y9zXwvFeN_XK2MnvcFQJXMiDsaw90130_provenance.
- NP80396.RAip9pKCyVcRtK17Y9zXwvFeN_XK2MnvcFQJXMiDsaw90130_assertion wasGeneratedBy ECO_0000203 NP80396.RAip9pKCyVcRtK17Y9zXwvFeN_XK2MnvcFQJXMiDsaw90130_provenance.
- gad-20150221 importedOn "2015-02-21" NP80396.RAip9pKCyVcRtK17Y9zXwvFeN_XK2MnvcFQJXMiDsaw90130_provenance.