Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP61465.RA94uRSf0VCC_U2_CRnLXQw5GDmMRHDGZblltc6IwqUAk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP61465.RA94uRSf0VCC_U2_CRnLXQw5GDmMRHDGZblltc6IwqUAk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP61465.RA94uRSf0VCC_U2_CRnLXQw5GDmMRHDGZblltc6IwqUAk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP61465.RA94uRSf0VCC_U2_CRnLXQw5GDmMRHDGZblltc6IwqUAk130_provenance.
- NP61465.RA94uRSf0VCC_U2_CRnLXQw5GDmMRHDGZblltc6IwqUAk130_assertion description "[In conclusion, the results of the present study provide evidence that C3435T MDR1 polymorphism may involve both the susceptibility to and the clinical outcome of childhood ALL. Carriers of the TT genotype are more at risk of developing ALL than other indi]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP61465.RA94uRSf0VCC_U2_CRnLXQw5GDmMRHDGZblltc6IwqUAk130_provenance.
- NP61465.RA94uRSf0VCC_U2_CRnLXQw5GDmMRHDGZblltc6IwqUAk130_assertion evidence source_evidence_literature NP61465.RA94uRSf0VCC_U2_CRnLXQw5GDmMRHDGZblltc6IwqUAk130_provenance.
- NP61465.RA94uRSf0VCC_U2_CRnLXQw5GDmMRHDGZblltc6IwqUAk130_assertion SIO_000772 15059065 NP61465.RA94uRSf0VCC_U2_CRnLXQw5GDmMRHDGZblltc6IwqUAk130_provenance.
- NP61465.RA94uRSf0VCC_U2_CRnLXQw5GDmMRHDGZblltc6IwqUAk130_assertion wasDerivedFrom gad-20150221 NP61465.RA94uRSf0VCC_U2_CRnLXQw5GDmMRHDGZblltc6IwqUAk130_provenance.
- NP61465.RA94uRSf0VCC_U2_CRnLXQw5GDmMRHDGZblltc6IwqUAk130_assertion wasGeneratedBy ECO_0000203 NP61465.RA94uRSf0VCC_U2_CRnLXQw5GDmMRHDGZblltc6IwqUAk130_provenance.
- gad-20150221 importedOn "2015-02-21" NP61465.RA94uRSf0VCC_U2_CRnLXQw5GDmMRHDGZblltc6IwqUAk130_provenance.