Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1042896.RAUlUCZsv9gpUEtn_SA__mdprwGD9-eAosdo2qgnpTC34130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1042896.RAUlUCZsv9gpUEtn_SA__mdprwGD9-eAosdo2qgnpTC34130_assertion type Assertion NP1042896.RAUlUCZsv9gpUEtn_SA__mdprwGD9-eAosdo2qgnpTC34130_head.
- NP1042896.RAUlUCZsv9gpUEtn_SA__mdprwGD9-eAosdo2qgnpTC34130_assertion description "[Cockayne Syndrome CS (Type A - CSA; or CS Type I OMIM #216400) (Type B - CSB; or CS Type II OMIM #133540) is a rare autosomal recessive neurological disease caused by defects in DNA repair characterized by progressive cachectic dwarfism, progressive intellectual disability with cerebral leukodystrophy, microcephaly, progressive pigmentary retinopathy, sensorineural deafness photosensitivity and possibly orofacial and dental anomalies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1042896.RAUlUCZsv9gpUEtn_SA__mdprwGD9-eAosdo2qgnpTC34130_provenance.
- NP1042896.RAUlUCZsv9gpUEtn_SA__mdprwGD9-eAosdo2qgnpTC34130_assertion evidence source_evidence_literature NP1042896.RAUlUCZsv9gpUEtn_SA__mdprwGD9-eAosdo2qgnpTC34130_provenance.
- NP1042896.RAUlUCZsv9gpUEtn_SA__mdprwGD9-eAosdo2qgnpTC34130_assertion SIO_000772 23311583 NP1042896.RAUlUCZsv9gpUEtn_SA__mdprwGD9-eAosdo2qgnpTC34130_provenance.
- NP1042896.RAUlUCZsv9gpUEtn_SA__mdprwGD9-eAosdo2qgnpTC34130_assertion wasDerivedFrom befree-2016 NP1042896.RAUlUCZsv9gpUEtn_SA__mdprwGD9-eAosdo2qgnpTC34130_provenance.
- NP1042896.RAUlUCZsv9gpUEtn_SA__mdprwGD9-eAosdo2qgnpTC34130_assertion wasGeneratedBy ECO_0000203 NP1042896.RAUlUCZsv9gpUEtn_SA__mdprwGD9-eAosdo2qgnpTC34130_provenance.