Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP237709.RASFVdvxei7ZVflHg39RVpe3x2WGDin--1Ni0dOetXGro130_assertion> ?p ?o ?g. }
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- NP237709.RASFVdvxei7ZVflHg39RVpe3x2WGDin--1Ni0dOetXGro130_assertion type Assertion NP237709.RASFVdvxei7ZVflHg39RVpe3x2WGDin--1Ni0dOetXGro130_head.
- NP237709.RASFVdvxei7ZVflHg39RVpe3x2WGDin--1Ni0dOetXGro130_assertion description "[The most severe form of the disease, X-linked centronuclear myopathy, is due to mutations in the gene encoding myotubularin (MTM1), while mutations in dynamin 2 (DNM2) and amphiphysin 2/BIN1 (AMPH2) cause milder forms of myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237709.RASFVdvxei7ZVflHg39RVpe3x2WGDin--1Ni0dOetXGro130_provenance.
- NP237709.RASFVdvxei7ZVflHg39RVpe3x2WGDin--1Ni0dOetXGro130_assertion evidence source_evidence_literature NP237709.RASFVdvxei7ZVflHg39RVpe3x2WGDin--1Ni0dOetXGro130_provenance.
- NP237709.RASFVdvxei7ZVflHg39RVpe3x2WGDin--1Ni0dOetXGro130_assertion SIO_000772 24569368 NP237709.RASFVdvxei7ZVflHg39RVpe3x2WGDin--1Ni0dOetXGro130_provenance.
- NP237709.RASFVdvxei7ZVflHg39RVpe3x2WGDin--1Ni0dOetXGro130_assertion wasDerivedFrom befree-20150227 NP237709.RASFVdvxei7ZVflHg39RVpe3x2WGDin--1Ni0dOetXGro130_provenance.
- NP237709.RASFVdvxei7ZVflHg39RVpe3x2WGDin--1Ni0dOetXGro130_assertion wasGeneratedBy ECO_0000203 NP237709.RASFVdvxei7ZVflHg39RVpe3x2WGDin--1Ni0dOetXGro130_provenance.