Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP525900.RAc0E1Sjy51pGfa-1ki_QR1omRZGNHZKVH7m9OibL8k-c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP525900.RAc0E1Sjy51pGfa-1ki_QR1omRZGNHZKVH7m9OibL8k-c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP525900.RAc0E1Sjy51pGfa-1ki_QR1omRZGNHZKVH7m9OibL8k-c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP525900.RAc0E1Sjy51pGfa-1ki_QR1omRZGNHZKVH7m9OibL8k-c130_provenance.
- NP525900.RAc0E1Sjy51pGfa-1ki_QR1omRZGNHZKVH7m9OibL8k-c130_assertion description "[A mutation in p89/XPB found in a xeroderma pigmentosum patient impairs the ability of TFIIH to associate correctly with the complex and thereby melt promoter DNA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP525900.RAc0E1Sjy51pGfa-1ki_QR1omRZGNHZKVH7m9OibL8k-c130_provenance.
- NP525900.RAc0E1Sjy51pGfa-1ki_QR1omRZGNHZKVH7m9OibL8k-c130_assertion evidence source_evidence_literature NP525900.RAc0E1Sjy51pGfa-1ki_QR1omRZGNHZKVH7m9OibL8k-c130_provenance.
- NP525900.RAc0E1Sjy51pGfa-1ki_QR1omRZGNHZKVH7m9OibL8k-c130_assertion SIO_000772 11027286 NP525900.RAc0E1Sjy51pGfa-1ki_QR1omRZGNHZKVH7m9OibL8k-c130_provenance.
- NP525900.RAc0E1Sjy51pGfa-1ki_QR1omRZGNHZKVH7m9OibL8k-c130_assertion wasDerivedFrom befree-20140225 NP525900.RAc0E1Sjy51pGfa-1ki_QR1omRZGNHZKVH7m9OibL8k-c130_provenance.
- NP525900.RAc0E1Sjy51pGfa-1ki_QR1omRZGNHZKVH7m9OibL8k-c130_assertion wasGeneratedBy ECO_0000203 NP525900.RAc0E1Sjy51pGfa-1ki_QR1omRZGNHZKVH7m9OibL8k-c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP525900.RAc0E1Sjy51pGfa-1ki_QR1omRZGNHZKVH7m9OibL8k-c130_provenance.