Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP151561.RAnXtfsMvvktIQDCAfAhd3hwV0llQTmJTkhPmSg4cf3YU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP151561.RAnXtfsMvvktIQDCAfAhd3hwV0llQTmJTkhPmSg4cf3YU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP151561.RAnXtfsMvvktIQDCAfAhd3hwV0llQTmJTkhPmSg4cf3YU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP151561.RAnXtfsMvvktIQDCAfAhd3hwV0llQTmJTkhPmSg4cf3YU130_provenance.
- NP151561.RAnXtfsMvvktIQDCAfAhd3hwV0llQTmJTkhPmSg4cf3YU130_assertion description "[These results suggest that individuals with homozygous deletion of GSTT1 and/or GSTM1 have a greater predisposition to vitiligo.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP151561.RAnXtfsMvvktIQDCAfAhd3hwV0llQTmJTkhPmSg4cf3YU130_provenance.
- NP151561.RAnXtfsMvvktIQDCAfAhd3hwV0llQTmJTkhPmSg4cf3YU130_assertion evidence source_evidence_literature NP151561.RAnXtfsMvvktIQDCAfAhd3hwV0llQTmJTkhPmSg4cf3YU130_provenance.
- NP151561.RAnXtfsMvvktIQDCAfAhd3hwV0llQTmJTkhPmSg4cf3YU130_assertion SIO_000772 19571817 NP151561.RAnXtfsMvvktIQDCAfAhd3hwV0llQTmJTkhPmSg4cf3YU130_provenance.
- NP151561.RAnXtfsMvvktIQDCAfAhd3hwV0llQTmJTkhPmSg4cf3YU130_assertion wasDerivedFrom gad-20150221 NP151561.RAnXtfsMvvktIQDCAfAhd3hwV0llQTmJTkhPmSg4cf3YU130_provenance.
- NP151561.RAnXtfsMvvktIQDCAfAhd3hwV0llQTmJTkhPmSg4cf3YU130_assertion wasGeneratedBy ECO_0000203 NP151561.RAnXtfsMvvktIQDCAfAhd3hwV0llQTmJTkhPmSg4cf3YU130_provenance.
- gad-20150221 importedOn "2015-02-21" NP151561.RAnXtfsMvvktIQDCAfAhd3hwV0llQTmJTkhPmSg4cf3YU130_provenance.