Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP2013.RAmvGCfFso3bMO8Q_tnXA_LefPxAtom0i9RFWFsdYsuqw130_assertion> ?p ?o ?g. }
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- NP2013.RAmvGCfFso3bMO8Q_tnXA_LefPxAtom0i9RFWFsdYsuqw130_assertion type Assertion NP2013.RAmvGCfFso3bMO8Q_tnXA_LefPxAtom0i9RFWFsdYsuqw130_head.
- NP2013.RAmvGCfFso3bMO8Q_tnXA_LefPxAtom0i9RFWFsdYsuqw130_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." NP2013.RAmvGCfFso3bMO8Q_tnXA_LefPxAtom0i9RFWFsdYsuqw130_provenance.
- NP2013.RAmvGCfFso3bMO8Q_tnXA_LefPxAtom0i9RFWFsdYsuqw130_assertion evidence source_evidence_curated NP2013.RAmvGCfFso3bMO8Q_tnXA_LefPxAtom0i9RFWFsdYsuqw130_provenance.
- NP2013.RAmvGCfFso3bMO8Q_tnXA_LefPxAtom0i9RFWFsdYsuqw130_assertion SIO_000772 9758621 NP2013.RAmvGCfFso3bMO8Q_tnXA_LefPxAtom0i9RFWFsdYsuqw130_provenance.
- NP2013.RAmvGCfFso3bMO8Q_tnXA_LefPxAtom0i9RFWFsdYsuqw130_assertion wasDerivedFrom uniprot-20130724 NP2013.RAmvGCfFso3bMO8Q_tnXA_LefPxAtom0i9RFWFsdYsuqw130_provenance.
- NP2013.RAmvGCfFso3bMO8Q_tnXA_LefPxAtom0i9RFWFsdYsuqw130_assertion wasGeneratedBy ECO_0000218 NP2013.RAmvGCfFso3bMO8Q_tnXA_LefPxAtom0i9RFWFsdYsuqw130_provenance.