Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP438392.RAC3SzwMBLx9Aufp6BBWbqckOHeJpU0W4INf1NtbU2nDc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP438392.RAC3SzwMBLx9Aufp6BBWbqckOHeJpU0W4INf1NtbU2nDc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP438392.RAC3SzwMBLx9Aufp6BBWbqckOHeJpU0W4INf1NtbU2nDc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP438392.RAC3SzwMBLx9Aufp6BBWbqckOHeJpU0W4INf1NtbU2nDc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP438392.RAC3SzwMBLx9Aufp6BBWbqckOHeJpU0W4INf1NtbU2nDc130_provenance.
- NP438392.RAC3SzwMBLx9Aufp6BBWbqckOHeJpU0W4INf1NtbU2nDc130_assertion wasGeneratedBy ECO_0000203 NP438392.RAC3SzwMBLx9Aufp6BBWbqckOHeJpU0W4INf1NtbU2nDc130_provenance.
- NP438392.RAC3SzwMBLx9Aufp6BBWbqckOHeJpU0W4INf1NtbU2nDc130_assertion wasDerivedFrom befree-20150227 NP438392.RAC3SzwMBLx9Aufp6BBWbqckOHeJpU0W4INf1NtbU2nDc130_provenance.
- NP438392.RAC3SzwMBLx9Aufp6BBWbqckOHeJpU0W4INf1NtbU2nDc130_assertion SIO_000772 22952149 NP438392.RAC3SzwMBLx9Aufp6BBWbqckOHeJpU0W4INf1NtbU2nDc130_provenance.
- NP438392.RAC3SzwMBLx9Aufp6BBWbqckOHeJpU0W4INf1NtbU2nDc130_assertion evidence source_evidence_literature NP438392.RAC3SzwMBLx9Aufp6BBWbqckOHeJpU0W4INf1NtbU2nDc130_provenance.
- NP438392.RAC3SzwMBLx9Aufp6BBWbqckOHeJpU0W4INf1NtbU2nDc130_assertion description "[Moreover, simultaneous carriage of both, the GSTM1 and the GSTT1 null genotypes, was almost identical in both groups (10.7% in GC vs. 10.6% in HC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP438392.RAC3SzwMBLx9Aufp6BBWbqckOHeJpU0W4INf1NtbU2nDc130_provenance.