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- NP381956.RA-2pPPClBxdNO-AZSknsDOr6tjsEBuciGOH2ahI7N1bc130_assertion type Assertion NP381956.RA-2pPPClBxdNO-AZSknsDOr6tjsEBuciGOH2ahI7N1bc130_head.
- NP381956.RA-2pPPClBxdNO-AZSknsDOr6tjsEBuciGOH2ahI7N1bc130_assertion description "[For the rare combined xeroderma pigmentosum (XP) and CS phenotype, all identified mutations are in three of the XP-associated genes, ERCC3 (XPB), ERCC2 (XPD), and ERCC5 (XPG).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP381956.RA-2pPPClBxdNO-AZSknsDOr6tjsEBuciGOH2ahI7N1bc130_provenance.
- NP381956.RA-2pPPClBxdNO-AZSknsDOr6tjsEBuciGOH2ahI7N1bc130_assertion evidence source_evidence_literature NP381956.RA-2pPPClBxdNO-AZSknsDOr6tjsEBuciGOH2ahI7N1bc130_provenance.
- NP381956.RA-2pPPClBxdNO-AZSknsDOr6tjsEBuciGOH2ahI7N1bc130_assertion SIO_000772 23623389 NP381956.RA-2pPPClBxdNO-AZSknsDOr6tjsEBuciGOH2ahI7N1bc130_provenance.
- NP381956.RA-2pPPClBxdNO-AZSknsDOr6tjsEBuciGOH2ahI7N1bc130_assertion wasDerivedFrom befree-20150227 NP381956.RA-2pPPClBxdNO-AZSknsDOr6tjsEBuciGOH2ahI7N1bc130_provenance.
- NP381956.RA-2pPPClBxdNO-AZSknsDOr6tjsEBuciGOH2ahI7N1bc130_assertion wasGeneratedBy ECO_0000203 NP381956.RA-2pPPClBxdNO-AZSknsDOr6tjsEBuciGOH2ahI7N1bc130_provenance.