Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP227918.RA8g3ZUuizNl74TGLLMoPsbRMg920lyDrb7cAH12mhp00130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP227918.RA8g3ZUuizNl74TGLLMoPsbRMg920lyDrb7cAH12mhp00130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP227918.RA8g3ZUuizNl74TGLLMoPsbRMg920lyDrb7cAH12mhp00130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP227918.RA8g3ZUuizNl74TGLLMoPsbRMg920lyDrb7cAH12mhp00130_provenance.
- NP227918.RA8g3ZUuizNl74TGLLMoPsbRMg920lyDrb7cAH12mhp00130_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." NP227918.RA8g3ZUuizNl74TGLLMoPsbRMg920lyDrb7cAH12mhp00130_provenance.
- NP227918.RA8g3ZUuizNl74TGLLMoPsbRMg920lyDrb7cAH12mhp00130_assertion evidence source_evidence_literature NP227918.RA8g3ZUuizNl74TGLLMoPsbRMg920lyDrb7cAH12mhp00130_provenance.
- NP227918.RA8g3ZUuizNl74TGLLMoPsbRMg920lyDrb7cAH12mhp00130_assertion SIO_000772 17676042 NP227918.RA8g3ZUuizNl74TGLLMoPsbRMg920lyDrb7cAH12mhp00130_provenance.
- NP227918.RA8g3ZUuizNl74TGLLMoPsbRMg920lyDrb7cAH12mhp00130_assertion wasDerivedFrom lhgdn-20090331 NP227918.RA8g3ZUuizNl74TGLLMoPsbRMg920lyDrb7cAH12mhp00130_provenance.
- NP227918.RA8g3ZUuizNl74TGLLMoPsbRMg920lyDrb7cAH12mhp00130_assertion wasGeneratedBy ECO_0000203 NP227918.RA8g3ZUuizNl74TGLLMoPsbRMg920lyDrb7cAH12mhp00130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP227918.RA8g3ZUuizNl74TGLLMoPsbRMg920lyDrb7cAH12mhp00130_provenance.