Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP143333.RAXExCHwSjU0_Y4Dp3ql4_FE2nmxy4ahPE4332eU9O9nk130_assertion> ?p ?o ?g. }
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- NP143333.RAXExCHwSjU0_Y4Dp3ql4_FE2nmxy4ahPE4332eU9O9nk130_assertion type Assertion NP143333.RAXExCHwSjU0_Y4Dp3ql4_FE2nmxy4ahPE4332eU9O9nk130_head.
- NP143333.RAXExCHwSjU0_Y4Dp3ql4_FE2nmxy4ahPE4332eU9O9nk130_assertion description "[Mutations in the myelin protein zero (MPZ) gene have been associated with different Charcot-Marie-Tooth disease (CMT) phenotypes, including classical demyelinating CMT1B and the axonal form of the disease (CMT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP143333.RAXExCHwSjU0_Y4Dp3ql4_FE2nmxy4ahPE4332eU9O9nk130_provenance.
- NP143333.RAXExCHwSjU0_Y4Dp3ql4_FE2nmxy4ahPE4332eU9O9nk130_assertion evidence source_evidence_literature NP143333.RAXExCHwSjU0_Y4Dp3ql4_FE2nmxy4ahPE4332eU9O9nk130_provenance.
- NP143333.RAXExCHwSjU0_Y4Dp3ql4_FE2nmxy4ahPE4332eU9O9nk130_assertion SIO_000772 19293842 NP143333.RAXExCHwSjU0_Y4Dp3ql4_FE2nmxy4ahPE4332eU9O9nk130_provenance.
- NP143333.RAXExCHwSjU0_Y4Dp3ql4_FE2nmxy4ahPE4332eU9O9nk130_assertion wasDerivedFrom gad-20150221 NP143333.RAXExCHwSjU0_Y4Dp3ql4_FE2nmxy4ahPE4332eU9O9nk130_provenance.
- NP143333.RAXExCHwSjU0_Y4Dp3ql4_FE2nmxy4ahPE4332eU9O9nk130_assertion wasGeneratedBy ECO_0000203 NP143333.RAXExCHwSjU0_Y4Dp3ql4_FE2nmxy4ahPE4332eU9O9nk130_provenance.