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- NP382722.RAvo9ovHyOfWqceHrHPMxcTe6fc6ouXcuBJJiJ6JDxb24130_assertion type Assertion NP382722.RAvo9ovHyOfWqceHrHPMxcTe6fc6ouXcuBJJiJ6JDxb24130_head.
- NP382722.RAvo9ovHyOfWqceHrHPMxcTe6fc6ouXcuBJJiJ6JDxb24130_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." NP382722.RAvo9ovHyOfWqceHrHPMxcTe6fc6ouXcuBJJiJ6JDxb24130_provenance.
- NP382722.RAvo9ovHyOfWqceHrHPMxcTe6fc6ouXcuBJJiJ6JDxb24130_assertion evidence source_evidence_literature NP382722.RAvo9ovHyOfWqceHrHPMxcTe6fc6ouXcuBJJiJ6JDxb24130_provenance.
- NP382722.RAvo9ovHyOfWqceHrHPMxcTe6fc6ouXcuBJJiJ6JDxb24130_assertion SIO_000772 23623389 NP382722.RAvo9ovHyOfWqceHrHPMxcTe6fc6ouXcuBJJiJ6JDxb24130_provenance.
- NP382722.RAvo9ovHyOfWqceHrHPMxcTe6fc6ouXcuBJJiJ6JDxb24130_assertion wasDerivedFrom befree-20150227 NP382722.RAvo9ovHyOfWqceHrHPMxcTe6fc6ouXcuBJJiJ6JDxb24130_provenance.
- NP382722.RAvo9ovHyOfWqceHrHPMxcTe6fc6ouXcuBJJiJ6JDxb24130_assertion wasGeneratedBy ECO_0000203 NP382722.RAvo9ovHyOfWqceHrHPMxcTe6fc6ouXcuBJJiJ6JDxb24130_provenance.