Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP415969.RAXtrjIwlyPEgRLx2suRDLejWmNe-8HUVR4p9yT-UOc8c130_assertion> ?p ?o ?g. }
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- NP415969.RAXtrjIwlyPEgRLx2suRDLejWmNe-8HUVR4p9yT-UOc8c130_assertion type Assertion NP415969.RAXtrjIwlyPEgRLx2suRDLejWmNe-8HUVR4p9yT-UOc8c130_head.
- NP415969.RAXtrjIwlyPEgRLx2suRDLejWmNe-8HUVR4p9yT-UOc8c130_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." NP415969.RAXtrjIwlyPEgRLx2suRDLejWmNe-8HUVR4p9yT-UOc8c130_provenance.
- NP415969.RAXtrjIwlyPEgRLx2suRDLejWmNe-8HUVR4p9yT-UOc8c130_assertion evidence source_evidence_literature NP415969.RAXtrjIwlyPEgRLx2suRDLejWmNe-8HUVR4p9yT-UOc8c130_provenance.
- NP415969.RAXtrjIwlyPEgRLx2suRDLejWmNe-8HUVR4p9yT-UOc8c130_assertion SIO_000772 14530412 NP415969.RAXtrjIwlyPEgRLx2suRDLejWmNe-8HUVR4p9yT-UOc8c130_provenance.
- NP415969.RAXtrjIwlyPEgRLx2suRDLejWmNe-8HUVR4p9yT-UOc8c130_assertion wasDerivedFrom befree-2016 NP415969.RAXtrjIwlyPEgRLx2suRDLejWmNe-8HUVR4p9yT-UOc8c130_provenance.
- NP415969.RAXtrjIwlyPEgRLx2suRDLejWmNe-8HUVR4p9yT-UOc8c130_assertion wasGeneratedBy ECO_0000203 NP415969.RAXtrjIwlyPEgRLx2suRDLejWmNe-8HUVR4p9yT-UOc8c130_provenance.