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- NP387281.RA8FXjfIWeTm80GsLh04mgLYjhm2METZpaVfb21VIV4lw130_assertion type Assertion NP387281.RA8FXjfIWeTm80GsLh04mgLYjhm2METZpaVfb21VIV4lw130_head.
- 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.