Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP716787.RAda0Ks_yL85tRObWaiO2JSYFv3jE-NgyaHAdeilXVmWs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP716787.RAda0Ks_yL85tRObWaiO2JSYFv3jE-NgyaHAdeilXVmWs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP716787.RAda0Ks_yL85tRObWaiO2JSYFv3jE-NgyaHAdeilXVmWs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP716787.RAda0Ks_yL85tRObWaiO2JSYFv3jE-NgyaHAdeilXVmWs130_provenance.
- befree-2016 importedOn "2016-02-19" NP716787.RAda0Ks_yL85tRObWaiO2JSYFv3jE-NgyaHAdeilXVmWs130_provenance.
- NP716787.RAda0Ks_yL85tRObWaiO2JSYFv3jE-NgyaHAdeilXVmWs130_assertion wasGeneratedBy ECO_0000203 NP716787.RAda0Ks_yL85tRObWaiO2JSYFv3jE-NgyaHAdeilXVmWs130_provenance.
- NP716787.RAda0Ks_yL85tRObWaiO2JSYFv3jE-NgyaHAdeilXVmWs130_assertion wasDerivedFrom befree-2016 NP716787.RAda0Ks_yL85tRObWaiO2JSYFv3jE-NgyaHAdeilXVmWs130_provenance.
- NP716787.RAda0Ks_yL85tRObWaiO2JSYFv3jE-NgyaHAdeilXVmWs130_assertion SIO_000772 19172752 NP716787.RAda0Ks_yL85tRObWaiO2JSYFv3jE-NgyaHAdeilXVmWs130_provenance.
- NP716787.RAda0Ks_yL85tRObWaiO2JSYFv3jE-NgyaHAdeilXVmWs130_assertion evidence source_evidence_literature NP716787.RAda0Ks_yL85tRObWaiO2JSYFv3jE-NgyaHAdeilXVmWs130_provenance.
- NP716787.RAda0Ks_yL85tRObWaiO2JSYFv3jE-NgyaHAdeilXVmWs130_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." NP716787.RAda0Ks_yL85tRObWaiO2JSYFv3jE-NgyaHAdeilXVmWs130_provenance.