Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP338249.RA3-f0pqTf0cmEo5UaDL-B8FHwu7CxL-dvEZfM-ESXfRA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP338249.RA3-f0pqTf0cmEo5UaDL-B8FHwu7CxL-dvEZfM-ESXfRA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP338249.RA3-f0pqTf0cmEo5UaDL-B8FHwu7CxL-dvEZfM-ESXfRA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP338249.RA3-f0pqTf0cmEo5UaDL-B8FHwu7CxL-dvEZfM-ESXfRA130_provenance.
- NP338249.RA3-f0pqTf0cmEo5UaDL-B8FHwu7CxL-dvEZfM-ESXfRA130_assertion description "[In this study, we tested whether null genotypes for the GSTM1 and GSTT1 genes altered the risks for MDS, AML and AA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP338249.RA3-f0pqTf0cmEo5UaDL-B8FHwu7CxL-dvEZfM-ESXfRA130_provenance.
- NP338249.RA3-f0pqTf0cmEo5UaDL-B8FHwu7CxL-dvEZfM-ESXfRA130_assertion evidence source_evidence_literature NP338249.RA3-f0pqTf0cmEo5UaDL-B8FHwu7CxL-dvEZfM-ESXfRA130_provenance.
- NP338249.RA3-f0pqTf0cmEo5UaDL-B8FHwu7CxL-dvEZfM-ESXfRA130_assertion SIO_000772 11488937 NP338249.RA3-f0pqTf0cmEo5UaDL-B8FHwu7CxL-dvEZfM-ESXfRA130_provenance.
- NP338249.RA3-f0pqTf0cmEo5UaDL-B8FHwu7CxL-dvEZfM-ESXfRA130_assertion wasDerivedFrom befree-20140225 NP338249.RA3-f0pqTf0cmEo5UaDL-B8FHwu7CxL-dvEZfM-ESXfRA130_provenance.
- NP338249.RA3-f0pqTf0cmEo5UaDL-B8FHwu7CxL-dvEZfM-ESXfRA130_assertion wasGeneratedBy ECO_0000203 NP338249.RA3-f0pqTf0cmEo5UaDL-B8FHwu7CxL-dvEZfM-ESXfRA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP338249.RA3-f0pqTf0cmEo5UaDL-B8FHwu7CxL-dvEZfM-ESXfRA130_provenance.