Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP387281.RA8FXjfIWeTm80GsLh04mgLYjhm2METZpaVfb21VIV4lw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP387281.RA8FXjfIWeTm80GsLh04mgLYjhm2METZpaVfb21VIV4lw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP387281.RA8FXjfIWeTm80GsLh04mgLYjhm2METZpaVfb21VIV4lw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP387281.RA8FXjfIWeTm80GsLh04mgLYjhm2METZpaVfb21VIV4lw130_provenance.
- NP387281.RA8FXjfIWeTm80GsLh04mgLYjhm2METZpaVfb21VIV4lw130_assertion description "[We have determined the mutations and the pattern of inheritance of the XPD alleles in the 11 cases identified in Italy so far, in which the hair abnormalities diagnostic for TTD are associated with different disease severity but similar cellular photosensitivity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP387281.RA8FXjfIWeTm80GsLh04mgLYjhm2METZpaVfb21VIV4lw130_provenance.
- NP387281.RA8FXjfIWeTm80GsLh04mgLYjhm2METZpaVfb21VIV4lw130_assertion evidence source_evidence_literature NP387281.RA8FXjfIWeTm80GsLh04mgLYjhm2METZpaVfb21VIV4lw130_provenance.
- NP387281.RA8FXjfIWeTm80GsLh04mgLYjhm2METZpaVfb21VIV4lw130_assertion SIO_000772 9758621 NP387281.RA8FXjfIWeTm80GsLh04mgLYjhm2METZpaVfb21VIV4lw130_provenance.
- NP387281.RA8FXjfIWeTm80GsLh04mgLYjhm2METZpaVfb21VIV4lw130_assertion wasDerivedFrom befree-20140225 NP387281.RA8FXjfIWeTm80GsLh04mgLYjhm2METZpaVfb21VIV4lw130_provenance.
- NP387281.RA8FXjfIWeTm80GsLh04mgLYjhm2METZpaVfb21VIV4lw130_assertion wasGeneratedBy ECO_0000203 NP387281.RA8FXjfIWeTm80GsLh04mgLYjhm2METZpaVfb21VIV4lw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP387281.RA8FXjfIWeTm80GsLh04mgLYjhm2METZpaVfb21VIV4lw130_provenance.