Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP560902.RA8g9K97Qgn_6BQJl4Yl_AVkN5fo5S8sLIZ8v-QtM-EhI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP560902.RA8g9K97Qgn_6BQJl4Yl_AVkN5fo5S8sLIZ8v-QtM-EhI130_assertion type Assertion NP560902.RA8g9K97Qgn_6BQJl4Yl_AVkN5fo5S8sLIZ8v-QtM-EhI130_head.
- NP560902.RA8g9K97Qgn_6BQJl4Yl_AVkN5fo5S8sLIZ8v-QtM-EhI130_assertion description "[In addition, this study is one of the largest GST polymorphism studies undertaken in the Spanish population and the first time that copy number variants have been scrutinized in relation to MM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP560902.RA8g9K97Qgn_6BQJl4Yl_AVkN5fo5S8sLIZ8v-QtM-EhI130_provenance.
- NP560902.RA8g9K97Qgn_6BQJl4Yl_AVkN5fo5S8sLIZ8v-QtM-EhI130_assertion evidence source_evidence_literature NP560902.RA8g9K97Qgn_6BQJl4Yl_AVkN5fo5S8sLIZ8v-QtM-EhI130_provenance.
- NP560902.RA8g9K97Qgn_6BQJl4Yl_AVkN5fo5S8sLIZ8v-QtM-EhI130_assertion SIO_000772 22251241 NP560902.RA8g9K97Qgn_6BQJl4Yl_AVkN5fo5S8sLIZ8v-QtM-EhI130_provenance.
- NP560902.RA8g9K97Qgn_6BQJl4Yl_AVkN5fo5S8sLIZ8v-QtM-EhI130_assertion wasDerivedFrom befree-20140225 NP560902.RA8g9K97Qgn_6BQJl4Yl_AVkN5fo5S8sLIZ8v-QtM-EhI130_provenance.
- NP560902.RA8g9K97Qgn_6BQJl4Yl_AVkN5fo5S8sLIZ8v-QtM-EhI130_assertion wasGeneratedBy ECO_0000203 NP560902.RA8g9K97Qgn_6BQJl4Yl_AVkN5fo5S8sLIZ8v-QtM-EhI130_provenance.