Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP810715.RAzqX-lhhOew-M6LdPg7zW6lr83qvH_Vo2dwmXfcpucSY130_assertion> ?p ?o ?g. }
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- NP810715.RAzqX-lhhOew-M6LdPg7zW6lr83qvH_Vo2dwmXfcpucSY130_assertion type Assertion NP810715.RAzqX-lhhOew-M6LdPg7zW6lr83qvH_Vo2dwmXfcpucSY130_head.
- NP810715.RAzqX-lhhOew-M6LdPg7zW6lr83qvH_Vo2dwmXfcpucSY130_assertion description "[Mutations in the myotubularin (MTM)-related protein 2 (MTMR2) gene are responsible for the severe autosomal recessive neuropathy Charcot-Marie-Tooth disease type 4B1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP810715.RAzqX-lhhOew-M6LdPg7zW6lr83qvH_Vo2dwmXfcpucSY130_provenance.
- NP810715.RAzqX-lhhOew-M6LdPg7zW6lr83qvH_Vo2dwmXfcpucSY130_assertion evidence source_evidence_literature NP810715.RAzqX-lhhOew-M6LdPg7zW6lr83qvH_Vo2dwmXfcpucSY130_provenance.
- NP810715.RAzqX-lhhOew-M6LdPg7zW6lr83qvH_Vo2dwmXfcpucSY130_assertion SIO_000772 14530412 NP810715.RAzqX-lhhOew-M6LdPg7zW6lr83qvH_Vo2dwmXfcpucSY130_provenance.
- NP810715.RAzqX-lhhOew-M6LdPg7zW6lr83qvH_Vo2dwmXfcpucSY130_assertion wasDerivedFrom befree-20150227 NP810715.RAzqX-lhhOew-M6LdPg7zW6lr83qvH_Vo2dwmXfcpucSY130_provenance.
- NP810715.RAzqX-lhhOew-M6LdPg7zW6lr83qvH_Vo2dwmXfcpucSY130_assertion wasGeneratedBy ECO_0000203 NP810715.RAzqX-lhhOew-M6LdPg7zW6lr83qvH_Vo2dwmXfcpucSY130_provenance.