Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1404987.RAYLTctmeXYR4termenLtQ80ZX3zH-50iVIA2MrXt-SEo130_assertion> ?p ?o ?g. }
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- NP1404987.RAYLTctmeXYR4termenLtQ80ZX3zH-50iVIA2MrXt-SEo130_assertion type Assertion NP1404987.RAYLTctmeXYR4termenLtQ80ZX3zH-50iVIA2MrXt-SEo130_head.
- NP1404987.RAYLTctmeXYR4termenLtQ80ZX3zH-50iVIA2MrXt-SEo130_assertion description "[Analysis of mutations in the XPD gene in Italian patients with trichothiodystrophy: site of mutation correlates with repair deficiency, but gene dosage appears to determine clinical severity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1404987.RAYLTctmeXYR4termenLtQ80ZX3zH-50iVIA2MrXt-SEo130_provenance.
- NP1404987.RAYLTctmeXYR4termenLtQ80ZX3zH-50iVIA2MrXt-SEo130_assertion evidence source_evidence_literature NP1404987.RAYLTctmeXYR4termenLtQ80ZX3zH-50iVIA2MrXt-SEo130_provenance.
- NP1404987.RAYLTctmeXYR4termenLtQ80ZX3zH-50iVIA2MrXt-SEo130_assertion SIO_000772 9758621 NP1404987.RAYLTctmeXYR4termenLtQ80ZX3zH-50iVIA2MrXt-SEo130_provenance.
- NP1404987.RAYLTctmeXYR4termenLtQ80ZX3zH-50iVIA2MrXt-SEo130_assertion wasDerivedFrom befree-2016 NP1404987.RAYLTctmeXYR4termenLtQ80ZX3zH-50iVIA2MrXt-SEo130_provenance.
- NP1404987.RAYLTctmeXYR4termenLtQ80ZX3zH-50iVIA2MrXt-SEo130_assertion wasGeneratedBy ECO_0000203 NP1404987.RAYLTctmeXYR4termenLtQ80ZX3zH-50iVIA2MrXt-SEo130_provenance.