Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP330094.RAqwGDUR8Y_jd5BhdRAXDIJrfA1CCgzE4P4lTy46ILkCg130_assertion> ?p ?o ?g. }
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- NP330094.RAqwGDUR8Y_jd5BhdRAXDIJrfA1CCgzE4P4lTy46ILkCg130_assertion type Assertion NP330094.RAqwGDUR8Y_jd5BhdRAXDIJrfA1CCgzE4P4lTy46ILkCg130_head.
- NP330094.RAqwGDUR8Y_jd5BhdRAXDIJrfA1CCgzE4P4lTy46ILkCg130_assertion wasGeneratedBy ECO_0000203 NP330094.RAqwGDUR8Y_jd5BhdRAXDIJrfA1CCgzE4P4lTy46ILkCg130_provenance.
- NP330094.RAqwGDUR8Y_jd5BhdRAXDIJrfA1CCgzE4P4lTy46ILkCg130_assertion wasDerivedFrom befree-20140225 NP330094.RAqwGDUR8Y_jd5BhdRAXDIJrfA1CCgzE4P4lTy46ILkCg130_provenance.
- NP330094.RAqwGDUR8Y_jd5BhdRAXDIJrfA1CCgzE4P4lTy46ILkCg130_assertion SIO_000772 9748047 NP330094.RAqwGDUR8Y_jd5BhdRAXDIJrfA1CCgzE4P4lTy46ILkCg130_provenance.
- NP330094.RAqwGDUR8Y_jd5BhdRAXDIJrfA1CCgzE4P4lTy46ILkCg130_assertion evidence source_evidence_literature NP330094.RAqwGDUR8Y_jd5BhdRAXDIJrfA1CCgzE4P4lTy46ILkCg130_provenance.
- NP330094.RAqwGDUR8Y_jd5BhdRAXDIJrfA1CCgzE4P4lTy46ILkCg130_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." NP330094.RAqwGDUR8Y_jd5BhdRAXDIJrfA1CCgzE4P4lTy46ILkCg130_provenance.