Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP900774.RACI79aeNx8yhsa9UMUQU1ErLSbjGg_V4ahj19vaYYXTw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP900774.RACI79aeNx8yhsa9UMUQU1ErLSbjGg_V4ahj19vaYYXTw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP900774.RACI79aeNx8yhsa9UMUQU1ErLSbjGg_V4ahj19vaYYXTw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP900774.RACI79aeNx8yhsa9UMUQU1ErLSbjGg_V4ahj19vaYYXTw130_provenance.
- NP900774.RACI79aeNx8yhsa9UMUQU1ErLSbjGg_V4ahj19vaYYXTw130_assertion description "[Patients with colon tumours and who were homozygous GSTT1(*)2 genotype carriers were more likely than patients who expressed GSTT1 to have their DNA alkylated (83 versus 32%, P=0.03) and to have higher O(6)-MedG levels (0.178+/-0.374 versus 0.016+/-0.023 micromol O(6)-MedG/mol dG, P=0.04) in normal, but not tumour, DNA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP900774.RACI79aeNx8yhsa9UMUQU1ErLSbjGg_V4ahj19vaYYXTw130_provenance.
- NP900774.RACI79aeNx8yhsa9UMUQU1ErLSbjGg_V4ahj19vaYYXTw130_assertion evidence source_evidence_literature NP900774.RACI79aeNx8yhsa9UMUQU1ErLSbjGg_V4ahj19vaYYXTw130_provenance.
- NP900774.RACI79aeNx8yhsa9UMUQU1ErLSbjGg_V4ahj19vaYYXTw130_assertion SIO_000772 11448648 NP900774.RACI79aeNx8yhsa9UMUQU1ErLSbjGg_V4ahj19vaYYXTw130_provenance.
- NP900774.RACI79aeNx8yhsa9UMUQU1ErLSbjGg_V4ahj19vaYYXTw130_assertion wasDerivedFrom befree-20140225 NP900774.RACI79aeNx8yhsa9UMUQU1ErLSbjGg_V4ahj19vaYYXTw130_provenance.
- NP900774.RACI79aeNx8yhsa9UMUQU1ErLSbjGg_V4ahj19vaYYXTw130_assertion wasGeneratedBy ECO_0000203 NP900774.RACI79aeNx8yhsa9UMUQU1ErLSbjGg_V4ahj19vaYYXTw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP900774.RACI79aeNx8yhsa9UMUQU1ErLSbjGg_V4ahj19vaYYXTw130_provenance.