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- NP936660.RAbliJljR8FTYmXRLuvvQpJ44mEU518Z_Kxhf-jSnPW5E130_assertion type Assertion NP936660.RAbliJljR8FTYmXRLuvvQpJ44mEU518Z_Kxhf-jSnPW5E130_head.
- NP936660.RAbliJljR8FTYmXRLuvvQpJ44mEU518Z_Kxhf-jSnPW5E130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936660.RAbliJljR8FTYmXRLuvvQpJ44mEU518Z_Kxhf-jSnPW5E130_provenance.
- NP936660.RAbliJljR8FTYmXRLuvvQpJ44mEU518Z_Kxhf-jSnPW5E130_assertion evidence source_evidence_literature NP936660.RAbliJljR8FTYmXRLuvvQpJ44mEU518Z_Kxhf-jSnPW5E130_provenance.
- NP936660.RAbliJljR8FTYmXRLuvvQpJ44mEU518Z_Kxhf-jSnPW5E130_assertion SIO_000772 10660593 NP936660.RAbliJljR8FTYmXRLuvvQpJ44mEU518Z_Kxhf-jSnPW5E130_provenance.
- NP936660.RAbliJljR8FTYmXRLuvvQpJ44mEU518Z_Kxhf-jSnPW5E130_assertion wasDerivedFrom befree-20140225 NP936660.RAbliJljR8FTYmXRLuvvQpJ44mEU518Z_Kxhf-jSnPW5E130_provenance.
- NP936660.RAbliJljR8FTYmXRLuvvQpJ44mEU518Z_Kxhf-jSnPW5E130_assertion wasGeneratedBy ECO_0000203 NP936660.RAbliJljR8FTYmXRLuvvQpJ44mEU518Z_Kxhf-jSnPW5E130_provenance.