Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP478109.RASDGuZF__wlTHdB7HNlAWgPInrV4UcDBbKQTZ7Nt5E2k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP478109.RASDGuZF__wlTHdB7HNlAWgPInrV4UcDBbKQTZ7Nt5E2k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP478109.RASDGuZF__wlTHdB7HNlAWgPInrV4UcDBbKQTZ7Nt5E2k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP478109.RASDGuZF__wlTHdB7HNlAWgPInrV4UcDBbKQTZ7Nt5E2k130_provenance.
- NP478109.RASDGuZF__wlTHdB7HNlAWgPInrV4UcDBbKQTZ7Nt5E2k130_assertion description "[GSTM1 deletion is significantly associated with the increased risk of symptomatic BPH, but none of the GST polymorphisms appears associated with response to standard BPH therapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478109.RASDGuZF__wlTHdB7HNlAWgPInrV4UcDBbKQTZ7Nt5E2k130_provenance.
- NP478109.RASDGuZF__wlTHdB7HNlAWgPInrV4UcDBbKQTZ7Nt5E2k130_assertion evidence source_evidence_literature NP478109.RASDGuZF__wlTHdB7HNlAWgPInrV4UcDBbKQTZ7Nt5E2k130_provenance.
- NP478109.RASDGuZF__wlTHdB7HNlAWgPInrV4UcDBbKQTZ7Nt5E2k130_assertion SIO_000772 21133626 NP478109.RASDGuZF__wlTHdB7HNlAWgPInrV4UcDBbKQTZ7Nt5E2k130_provenance.
- NP478109.RASDGuZF__wlTHdB7HNlAWgPInrV4UcDBbKQTZ7Nt5E2k130_assertion wasDerivedFrom befree-20140225 NP478109.RASDGuZF__wlTHdB7HNlAWgPInrV4UcDBbKQTZ7Nt5E2k130_provenance.
- NP478109.RASDGuZF__wlTHdB7HNlAWgPInrV4UcDBbKQTZ7Nt5E2k130_assertion wasGeneratedBy ECO_0000203 NP478109.RASDGuZF__wlTHdB7HNlAWgPInrV4UcDBbKQTZ7Nt5E2k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP478109.RASDGuZF__wlTHdB7HNlAWgPInrV4UcDBbKQTZ7Nt5E2k130_provenance.