Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP584661.RAE8Fw_GKq-YLpVGNft1E78JtmGUaa3VCSlfEH6orJDGk130_assertion> ?p ?o ?g. }
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- NP584661.RAE8Fw_GKq-YLpVGNft1E78JtmGUaa3VCSlfEH6orJDGk130_assertion type Assertion NP584661.RAE8Fw_GKq-YLpVGNft1E78JtmGUaa3VCSlfEH6orJDGk130_head.
- NP584661.RAE8Fw_GKq-YLpVGNft1E78JtmGUaa3VCSlfEH6orJDGk130_assertion wasGeneratedBy ECO_0000203 NP584661.RAE8Fw_GKq-YLpVGNft1E78JtmGUaa3VCSlfEH6orJDGk130_provenance.
- NP584661.RAE8Fw_GKq-YLpVGNft1E78JtmGUaa3VCSlfEH6orJDGk130_assertion wasDerivedFrom befree-20150227 NP584661.RAE8Fw_GKq-YLpVGNft1E78JtmGUaa3VCSlfEH6orJDGk130_provenance.
- NP584661.RAE8Fw_GKq-YLpVGNft1E78JtmGUaa3VCSlfEH6orJDGk130_assertion SIO_000772 9748047 NP584661.RAE8Fw_GKq-YLpVGNft1E78JtmGUaa3VCSlfEH6orJDGk130_provenance.
- NP584661.RAE8Fw_GKq-YLpVGNft1E78JtmGUaa3VCSlfEH6orJDGk130_assertion evidence source_evidence_literature NP584661.RAE8Fw_GKq-YLpVGNft1E78JtmGUaa3VCSlfEH6orJDGk130_provenance.
- NP584661.RAE8Fw_GKq-YLpVGNft1E78JtmGUaa3VCSlfEH6orJDGk130_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." NP584661.RAE8Fw_GKq-YLpVGNft1E78JtmGUaa3VCSlfEH6orJDGk130_provenance.