Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP560902.RA8g9K97Qgn_6BQJl4Yl_AVkN5fo5S8sLIZ8v-QtM-EhI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP560902.RA8g9K97Qgn_6BQJl4Yl_AVkN5fo5S8sLIZ8v-QtM-EhI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP560902.RA8g9K97Qgn_6BQJl4Yl_AVkN5fo5S8sLIZ8v-QtM-EhI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP560902.RA8g9K97Qgn_6BQJl4Yl_AVkN5fo5S8sLIZ8v-QtM-EhI130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP560902.RA8g9K97Qgn_6BQJl4Yl_AVkN5fo5S8sLIZ8v-QtM-EhI130_provenance.