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- source_evidence_literature type ECO_0000212 NP748813.RA8Z2LOFA-lmlgqEDZh_427G1z-gJzEbIZDkgWu7nxrxM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP748813.RA8Z2LOFA-lmlgqEDZh_427G1z-gJzEbIZDkgWu7nxrxM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP748813.RA8Z2LOFA-lmlgqEDZh_427G1z-gJzEbIZDkgWu7nxrxM130_provenance.
- NP748813.RA8Z2LOFA-lmlgqEDZh_427G1z-gJzEbIZDkgWu7nxrxM130_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." NP748813.RA8Z2LOFA-lmlgqEDZh_427G1z-gJzEbIZDkgWu7nxrxM130_provenance.
- NP748813.RA8Z2LOFA-lmlgqEDZh_427G1z-gJzEbIZDkgWu7nxrxM130_assertion evidence source_evidence_literature NP748813.RA8Z2LOFA-lmlgqEDZh_427G1z-gJzEbIZDkgWu7nxrxM130_provenance.
- NP748813.RA8Z2LOFA-lmlgqEDZh_427G1z-gJzEbIZDkgWu7nxrxM130_assertion SIO_000772 19571817 NP748813.RA8Z2LOFA-lmlgqEDZh_427G1z-gJzEbIZDkgWu7nxrxM130_provenance.
- NP748813.RA8Z2LOFA-lmlgqEDZh_427G1z-gJzEbIZDkgWu7nxrxM130_assertion wasDerivedFrom befree-2016 NP748813.RA8Z2LOFA-lmlgqEDZh_427G1z-gJzEbIZDkgWu7nxrxM130_provenance.
- NP748813.RA8Z2LOFA-lmlgqEDZh_427G1z-gJzEbIZDkgWu7nxrxM130_assertion wasGeneratedBy ECO_0000203 NP748813.RA8Z2LOFA-lmlgqEDZh_427G1z-gJzEbIZDkgWu7nxrxM130_provenance.
- befree-2016 importedOn "2016-02-19" NP748813.RA8Z2LOFA-lmlgqEDZh_427G1z-gJzEbIZDkgWu7nxrxM130_provenance.