Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP102784.RAl_hui2-t1scVVhb-moIx27KwBKongQe30FuopR0EWC4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP102784.RAl_hui2-t1scVVhb-moIx27KwBKongQe30FuopR0EWC4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP102784.RAl_hui2-t1scVVhb-moIx27KwBKongQe30FuopR0EWC4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP102784.RAl_hui2-t1scVVhb-moIx27KwBKongQe30FuopR0EWC4130_provenance.
- NP102784.RAl_hui2-t1scVVhb-moIx27KwBKongQe30FuopR0EWC4130_assertion description "[The GSTP1 codon 105 polymorphism, but not GSTM1 or GSTT1 null mutations, significantly increased the risks of short-term side-effects of pulsed high-dose CTX therapy in SLE patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP102784.RAl_hui2-t1scVVhb-moIx27KwBKongQe30FuopR0EWC4130_provenance.
- NP102784.RAl_hui2-t1scVVhb-moIx27KwBKongQe30FuopR0EWC4130_assertion evidence source_evidence_literature NP102784.RAl_hui2-t1scVVhb-moIx27KwBKongQe30FuopR0EWC4130_provenance.
- NP102784.RAl_hui2-t1scVVhb-moIx27KwBKongQe30FuopR0EWC4130_assertion SIO_000772 16995867 NP102784.RAl_hui2-t1scVVhb-moIx27KwBKongQe30FuopR0EWC4130_provenance.
- NP102784.RAl_hui2-t1scVVhb-moIx27KwBKongQe30FuopR0EWC4130_assertion wasDerivedFrom gad-20150221 NP102784.RAl_hui2-t1scVVhb-moIx27KwBKongQe30FuopR0EWC4130_provenance.
- NP102784.RAl_hui2-t1scVVhb-moIx27KwBKongQe30FuopR0EWC4130_assertion wasGeneratedBy ECO_0000203 NP102784.RAl_hui2-t1scVVhb-moIx27KwBKongQe30FuopR0EWC4130_provenance.
- gad-20150221 importedOn "2015-02-21" NP102784.RAl_hui2-t1scVVhb-moIx27KwBKongQe30FuopR0EWC4130_provenance.