Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP315750.RA_LyYpbxuRT2M2rf9K9Hqo_9o2ocayPrE3T1mikgyeDM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP315750.RA_LyYpbxuRT2M2rf9K9Hqo_9o2ocayPrE3T1mikgyeDM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP315750.RA_LyYpbxuRT2M2rf9K9Hqo_9o2ocayPrE3T1mikgyeDM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP315750.RA_LyYpbxuRT2M2rf9K9Hqo_9o2ocayPrE3T1mikgyeDM130_provenance.
- NP315750.RA_LyYpbxuRT2M2rf9K9Hqo_9o2ocayPrE3T1mikgyeDM130_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." NP315750.RA_LyYpbxuRT2M2rf9K9Hqo_9o2ocayPrE3T1mikgyeDM130_provenance.
- NP315750.RA_LyYpbxuRT2M2rf9K9Hqo_9o2ocayPrE3T1mikgyeDM130_assertion evidence source_evidence_literature NP315750.RA_LyYpbxuRT2M2rf9K9Hqo_9o2ocayPrE3T1mikgyeDM130_provenance.
- NP315750.RA_LyYpbxuRT2M2rf9K9Hqo_9o2ocayPrE3T1mikgyeDM130_assertion SIO_000772 10660593 NP315750.RA_LyYpbxuRT2M2rf9K9Hqo_9o2ocayPrE3T1mikgyeDM130_provenance.
- NP315750.RA_LyYpbxuRT2M2rf9K9Hqo_9o2ocayPrE3T1mikgyeDM130_assertion wasDerivedFrom befree-20140225 NP315750.RA_LyYpbxuRT2M2rf9K9Hqo_9o2ocayPrE3T1mikgyeDM130_provenance.
- NP315750.RA_LyYpbxuRT2M2rf9K9Hqo_9o2ocayPrE3T1mikgyeDM130_assertion wasGeneratedBy ECO_0000203 NP315750.RA_LyYpbxuRT2M2rf9K9Hqo_9o2ocayPrE3T1mikgyeDM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP315750.RA_LyYpbxuRT2M2rf9K9Hqo_9o2ocayPrE3T1mikgyeDM130_provenance.