Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP817001.RA8MDo5e0Z71WLBeClPgN8pHHFE-aCrOQWD-bFAgCUmto130_assertion> ?p ?o ?g. }
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- NP817001.RA8MDo5e0Z71WLBeClPgN8pHHFE-aCrOQWD-bFAgCUmto130_assertion type Assertion NP817001.RA8MDo5e0Z71WLBeClPgN8pHHFE-aCrOQWD-bFAgCUmto130_head.
- NP817001.RA8MDo5e0Z71WLBeClPgN8pHHFE-aCrOQWD-bFAgCUmto130_assertion description "[A novel AP4M1 mutation in autosomal recessive cerebral palsy syndrome and clinical expansion of AP-4 deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP817001.RA8MDo5e0Z71WLBeClPgN8pHHFE-aCrOQWD-bFAgCUmto130_provenance.
- NP817001.RA8MDo5e0Z71WLBeClPgN8pHHFE-aCrOQWD-bFAgCUmto130_assertion evidence source_evidence_literature NP817001.RA8MDo5e0Z71WLBeClPgN8pHHFE-aCrOQWD-bFAgCUmto130_provenance.
- NP817001.RA8MDo5e0Z71WLBeClPgN8pHHFE-aCrOQWD-bFAgCUmto130_assertion SIO_000772 25496299 NP817001.RA8MDo5e0Z71WLBeClPgN8pHHFE-aCrOQWD-bFAgCUmto130_provenance.
- NP817001.RA8MDo5e0Z71WLBeClPgN8pHHFE-aCrOQWD-bFAgCUmto130_assertion wasDerivedFrom befree-20150227 NP817001.RA8MDo5e0Z71WLBeClPgN8pHHFE-aCrOQWD-bFAgCUmto130_provenance.
- NP817001.RA8MDo5e0Z71WLBeClPgN8pHHFE-aCrOQWD-bFAgCUmto130_assertion wasGeneratedBy ECO_0000203 NP817001.RA8MDo5e0Z71WLBeClPgN8pHHFE-aCrOQWD-bFAgCUmto130_provenance.