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- source_evidence_literature type ECO_0000212 NP866951.RA2JL-FRqRjPuG_TzUBjAxXEDPhfulbq7tzYJtly0indw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP866951.RA2JL-FRqRjPuG_TzUBjAxXEDPhfulbq7tzYJtly0indw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP866951.RA2JL-FRqRjPuG_TzUBjAxXEDPhfulbq7tzYJtly0indw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP866951.RA2JL-FRqRjPuG_TzUBjAxXEDPhfulbq7tzYJtly0indw130_provenance.
- NP866951.RA2JL-FRqRjPuG_TzUBjAxXEDPhfulbq7tzYJtly0indw130_assertion wasGeneratedBy ECO_0000203 NP866951.RA2JL-FRqRjPuG_TzUBjAxXEDPhfulbq7tzYJtly0indw130_provenance.
- NP866951.RA2JL-FRqRjPuG_TzUBjAxXEDPhfulbq7tzYJtly0indw130_assertion wasDerivedFrom befree-20150227 NP866951.RA2JL-FRqRjPuG_TzUBjAxXEDPhfulbq7tzYJtly0indw130_provenance.
- NP866951.RA2JL-FRqRjPuG_TzUBjAxXEDPhfulbq7tzYJtly0indw130_assertion SIO_000772 19172752 NP866951.RA2JL-FRqRjPuG_TzUBjAxXEDPhfulbq7tzYJtly0indw130_provenance.
- NP866951.RA2JL-FRqRjPuG_TzUBjAxXEDPhfulbq7tzYJtly0indw130_assertion evidence source_evidence_literature NP866951.RA2JL-FRqRjPuG_TzUBjAxXEDPhfulbq7tzYJtly0indw130_provenance.
- NP866951.RA2JL-FRqRjPuG_TzUBjAxXEDPhfulbq7tzYJtly0indw130_assertion description "[Patients with the rare neurodevelopmental repair syndrome known as group A trichothiodystrophy (TTD-A) carry mutations in the gene encoding the p8 subunit of the transcription and DNA repair factor TFIIH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP866951.RA2JL-FRqRjPuG_TzUBjAxXEDPhfulbq7tzYJtly0indw130_provenance.