Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP817001.RA8MDo5e0Z71WLBeClPgN8pHHFE-aCrOQWD-bFAgCUmto130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP817001.RA8MDo5e0Z71WLBeClPgN8pHHFE-aCrOQWD-bFAgCUmto130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP817001.RA8MDo5e0Z71WLBeClPgN8pHHFE-aCrOQWD-bFAgCUmto130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP817001.RA8MDo5e0Z71WLBeClPgN8pHHFE-aCrOQWD-bFAgCUmto130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP817001.RA8MDo5e0Z71WLBeClPgN8pHHFE-aCrOQWD-bFAgCUmto130_provenance.