Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP143306.RAMeHEDmt3K0lyw9cYX1nMrADtVWYF8sfuQko-j2JftVw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP143306.RAMeHEDmt3K0lyw9cYX1nMrADtVWYF8sfuQko-j2JftVw130_assertion type Assertion NP143306.RAMeHEDmt3K0lyw9cYX1nMrADtVWYF8sfuQko-j2JftVw130_head.
- NP143306.RAMeHEDmt3K0lyw9cYX1nMrADtVWYF8sfuQko-j2JftVw130_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." NP143306.RAMeHEDmt3K0lyw9cYX1nMrADtVWYF8sfuQko-j2JftVw130_provenance.
- NP143306.RAMeHEDmt3K0lyw9cYX1nMrADtVWYF8sfuQko-j2JftVw130_assertion evidence source_evidence_literature NP143306.RAMeHEDmt3K0lyw9cYX1nMrADtVWYF8sfuQko-j2JftVw130_provenance.
- NP143306.RAMeHEDmt3K0lyw9cYX1nMrADtVWYF8sfuQko-j2JftVw130_assertion SIO_000772 15059065 NP143306.RAMeHEDmt3K0lyw9cYX1nMrADtVWYF8sfuQko-j2JftVw130_provenance.
- NP143306.RAMeHEDmt3K0lyw9cYX1nMrADtVWYF8sfuQko-j2JftVw130_assertion wasDerivedFrom lhgdn-20090331 NP143306.RAMeHEDmt3K0lyw9cYX1nMrADtVWYF8sfuQko-j2JftVw130_provenance.
- NP143306.RAMeHEDmt3K0lyw9cYX1nMrADtVWYF8sfuQko-j2JftVw130_assertion wasGeneratedBy ECO_0000203 NP143306.RAMeHEDmt3K0lyw9cYX1nMrADtVWYF8sfuQko-j2JftVw130_provenance.