Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP582338.RAEVPUFuLw8cCjd1o7Sa1Bo_bCi6w7ZVn3tg4rKjmsh24130_assertion> ?p ?o ?g. }
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- NP582338.RAEVPUFuLw8cCjd1o7Sa1Bo_bCi6w7ZVn3tg4rKjmsh24130_assertion type Assertion NP582338.RAEVPUFuLw8cCjd1o7Sa1Bo_bCi6w7ZVn3tg4rKjmsh24130_head.
- NP582338.RAEVPUFuLw8cCjd1o7Sa1Bo_bCi6w7ZVn3tg4rKjmsh24130_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." NP582338.RAEVPUFuLw8cCjd1o7Sa1Bo_bCi6w7ZVn3tg4rKjmsh24130_provenance.
- NP582338.RAEVPUFuLw8cCjd1o7Sa1Bo_bCi6w7ZVn3tg4rKjmsh24130_assertion evidence source_evidence_literature NP582338.RAEVPUFuLw8cCjd1o7Sa1Bo_bCi6w7ZVn3tg4rKjmsh24130_provenance.
- NP582338.RAEVPUFuLw8cCjd1o7Sa1Bo_bCi6w7ZVn3tg4rKjmsh24130_assertion SIO_000772 11955452 NP582338.RAEVPUFuLw8cCjd1o7Sa1Bo_bCi6w7ZVn3tg4rKjmsh24130_provenance.
- NP582338.RAEVPUFuLw8cCjd1o7Sa1Bo_bCi6w7ZVn3tg4rKjmsh24130_assertion wasDerivedFrom befree-20140225 NP582338.RAEVPUFuLw8cCjd1o7Sa1Bo_bCi6w7ZVn3tg4rKjmsh24130_provenance.
- NP582338.RAEVPUFuLw8cCjd1o7Sa1Bo_bCi6w7ZVn3tg4rKjmsh24130_assertion wasGeneratedBy ECO_0000203 NP582338.RAEVPUFuLw8cCjd1o7Sa1Bo_bCi6w7ZVn3tg4rKjmsh24130_provenance.