Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1404522.RAKRddGvOFb_6TDkbLc90i-jC3K2wuFg8u5f4R_as6wMQ130_assertion> ?p ?o ?g. }
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- NP1404522.RAKRddGvOFb_6TDkbLc90i-jC3K2wuFg8u5f4R_as6wMQ130_assertion type Assertion NP1404522.RAKRddGvOFb_6TDkbLc90i-jC3K2wuFg8u5f4R_as6wMQ130_head.
- NP1404522.RAKRddGvOFb_6TDkbLc90i-jC3K2wuFg8u5f4R_as6wMQ130_assertion wasGeneratedBy ECO_0000203 NP1404522.RAKRddGvOFb_6TDkbLc90i-jC3K2wuFg8u5f4R_as6wMQ130_provenance.
- NP1404522.RAKRddGvOFb_6TDkbLc90i-jC3K2wuFg8u5f4R_as6wMQ130_assertion wasDerivedFrom befree-2016 NP1404522.RAKRddGvOFb_6TDkbLc90i-jC3K2wuFg8u5f4R_as6wMQ130_provenance.
- NP1404522.RAKRddGvOFb_6TDkbLc90i-jC3K2wuFg8u5f4R_as6wMQ130_assertion SIO_000772 9748047 NP1404522.RAKRddGvOFb_6TDkbLc90i-jC3K2wuFg8u5f4R_as6wMQ130_provenance.
- NP1404522.RAKRddGvOFb_6TDkbLc90i-jC3K2wuFg8u5f4R_as6wMQ130_assertion evidence source_evidence_literature NP1404522.RAKRddGvOFb_6TDkbLc90i-jC3K2wuFg8u5f4R_as6wMQ130_provenance.
- NP1404522.RAKRddGvOFb_6TDkbLc90i-jC3K2wuFg8u5f4R_as6wMQ130_assertion description "[A Chinese male infant with arthrogryposis multiplex congenita (AMC), ventricular and atrial septal defects, and Werdnig-Hoffmann disease (WHD) had deletions of the telomeric copy of the survival motor neuron (SMN(T)) and neuronal apoptosis inhibitory protein genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1404522.RAKRddGvOFb_6TDkbLc90i-jC3K2wuFg8u5f4R_as6wMQ130_provenance.