Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP205326.RAXMlnhWX9lRGJe6pqK_dZ1_jj0UGGLUzvjGqYNFjk5cE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP205326.RAXMlnhWX9lRGJe6pqK_dZ1_jj0UGGLUzvjGqYNFjk5cE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP205326.RAXMlnhWX9lRGJe6pqK_dZ1_jj0UGGLUzvjGqYNFjk5cE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP205326.RAXMlnhWX9lRGJe6pqK_dZ1_jj0UGGLUzvjGqYNFjk5cE130_provenance.
- NP205326.RAXMlnhWX9lRGJe6pqK_dZ1_jj0UGGLUzvjGqYNFjk5cE130_assertion description "[Mutations in amphiphysin 2 (BIN1) disrupt its membrane tubulation properties and its interaction with dynamin 2, and cause autosomal recessive centronuclear myopathy]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205326.RAXMlnhWX9lRGJe6pqK_dZ1_jj0UGGLUzvjGqYNFjk5cE130_provenance.
- NP205326.RAXMlnhWX9lRGJe6pqK_dZ1_jj0UGGLUzvjGqYNFjk5cE130_assertion evidence source_evidence_literature NP205326.RAXMlnhWX9lRGJe6pqK_dZ1_jj0UGGLUzvjGqYNFjk5cE130_provenance.
- NP205326.RAXMlnhWX9lRGJe6pqK_dZ1_jj0UGGLUzvjGqYNFjk5cE130_assertion SIO_000772 17676042 NP205326.RAXMlnhWX9lRGJe6pqK_dZ1_jj0UGGLUzvjGqYNFjk5cE130_provenance.
- NP205326.RAXMlnhWX9lRGJe6pqK_dZ1_jj0UGGLUzvjGqYNFjk5cE130_assertion wasDerivedFrom lhgdn-20090331 NP205326.RAXMlnhWX9lRGJe6pqK_dZ1_jj0UGGLUzvjGqYNFjk5cE130_provenance.
- NP205326.RAXMlnhWX9lRGJe6pqK_dZ1_jj0UGGLUzvjGqYNFjk5cE130_assertion wasGeneratedBy ECO_0000203 NP205326.RAXMlnhWX9lRGJe6pqK_dZ1_jj0UGGLUzvjGqYNFjk5cE130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP205326.RAXMlnhWX9lRGJe6pqK_dZ1_jj0UGGLUzvjGqYNFjk5cE130_provenance.