Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP441802.RA9195xLldo_tMQMPizawdfpV0XhMG6OPHhFimnpSYt9g130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP441802.RA9195xLldo_tMQMPizawdfpV0XhMG6OPHhFimnpSYt9g130_assertion type Assertion NP441802.RA9195xLldo_tMQMPizawdfpV0XhMG6OPHhFimnpSYt9g130_head.
- NP441802.RA9195xLldo_tMQMPizawdfpV0XhMG6OPHhFimnpSYt9g130_assertion wasGeneratedBy ECO_0000203 NP441802.RA9195xLldo_tMQMPizawdfpV0XhMG6OPHhFimnpSYt9g130_provenance.
- NP441802.RA9195xLldo_tMQMPizawdfpV0XhMG6OPHhFimnpSYt9g130_assertion wasDerivedFrom befree-20150227 NP441802.RA9195xLldo_tMQMPizawdfpV0XhMG6OPHhFimnpSYt9g130_provenance.
- NP441802.RA9195xLldo_tMQMPizawdfpV0XhMG6OPHhFimnpSYt9g130_assertion SIO_000772 19172752 NP441802.RA9195xLldo_tMQMPizawdfpV0XhMG6OPHhFimnpSYt9g130_provenance.
- NP441802.RA9195xLldo_tMQMPizawdfpV0XhMG6OPHhFimnpSYt9g130_assertion evidence source_evidence_literature NP441802.RA9195xLldo_tMQMPizawdfpV0XhMG6OPHhFimnpSYt9g130_provenance.
- NP441802.RA9195xLldo_tMQMPizawdfpV0XhMG6OPHhFimnpSYt9g130_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." NP441802.RA9195xLldo_tMQMPizawdfpV0XhMG6OPHhFimnpSYt9g130_provenance.