Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP184672.RAUN8VsyEGs3zs2LC43x3Eponumrm3HfOHNLbW92zGxqg130_assertion> ?p ?o ?g. }
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- NP184672.RAUN8VsyEGs3zs2LC43x3Eponumrm3HfOHNLbW92zGxqg130_assertion type Assertion NP184672.RAUN8VsyEGs3zs2LC43x3Eponumrm3HfOHNLbW92zGxqg130_head.
- NP184672.RAUN8VsyEGs3zs2LC43x3Eponumrm3HfOHNLbW92zGxqg130_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." NP184672.RAUN8VsyEGs3zs2LC43x3Eponumrm3HfOHNLbW92zGxqg130_provenance.
- NP184672.RAUN8VsyEGs3zs2LC43x3Eponumrm3HfOHNLbW92zGxqg130_assertion evidence source_evidence_literature NP184672.RAUN8VsyEGs3zs2LC43x3Eponumrm3HfOHNLbW92zGxqg130_provenance.
- NP184672.RAUN8VsyEGs3zs2LC43x3Eponumrm3HfOHNLbW92zGxqg130_assertion SIO_000772 10660593 NP184672.RAUN8VsyEGs3zs2LC43x3Eponumrm3HfOHNLbW92zGxqg130_provenance.
- NP184672.RAUN8VsyEGs3zs2LC43x3Eponumrm3HfOHNLbW92zGxqg130_assertion wasDerivedFrom befree-20140225 NP184672.RAUN8VsyEGs3zs2LC43x3Eponumrm3HfOHNLbW92zGxqg130_provenance.
- NP184672.RAUN8VsyEGs3zs2LC43x3Eponumrm3HfOHNLbW92zGxqg130_assertion wasGeneratedBy ECO_0000203 NP184672.RAUN8VsyEGs3zs2LC43x3Eponumrm3HfOHNLbW92zGxqg130_provenance.