Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1011273.RAJqv-EqFyuZjWa_Kj6gTv17eVrSdDpNhGmx0ioubdHEM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1011273.RAJqv-EqFyuZjWa_Kj6gTv17eVrSdDpNhGmx0ioubdHEM130_assertion type Assertion NP1011273.RAJqv-EqFyuZjWa_Kj6gTv17eVrSdDpNhGmx0ioubdHEM130_head.
- NP1011273.RAJqv-EqFyuZjWa_Kj6gTv17eVrSdDpNhGmx0ioubdHEM130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1011273.RAJqv-EqFyuZjWa_Kj6gTv17eVrSdDpNhGmx0ioubdHEM130_provenance.
- NP1011273.RAJqv-EqFyuZjWa_Kj6gTv17eVrSdDpNhGmx0ioubdHEM130_assertion evidence source_evidence_literature NP1011273.RAJqv-EqFyuZjWa_Kj6gTv17eVrSdDpNhGmx0ioubdHEM130_provenance.
- NP1011273.RAJqv-EqFyuZjWa_Kj6gTv17eVrSdDpNhGmx0ioubdHEM130_assertion SIO_000772 11955452 NP1011273.RAJqv-EqFyuZjWa_Kj6gTv17eVrSdDpNhGmx0ioubdHEM130_provenance.
- NP1011273.RAJqv-EqFyuZjWa_Kj6gTv17eVrSdDpNhGmx0ioubdHEM130_assertion wasDerivedFrom befree-20150227 NP1011273.RAJqv-EqFyuZjWa_Kj6gTv17eVrSdDpNhGmx0ioubdHEM130_provenance.
- NP1011273.RAJqv-EqFyuZjWa_Kj6gTv17eVrSdDpNhGmx0ioubdHEM130_assertion wasGeneratedBy ECO_0000203 NP1011273.RAJqv-EqFyuZjWa_Kj6gTv17eVrSdDpNhGmx0ioubdHEM130_provenance.