Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP947288.RAkrJB7D1Q2oaDtDZIbANak9lHM3CCXf5kZ1T3bAFv-v8130_assertion> ?p ?o ?g. }
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- NP947288.RAkrJB7D1Q2oaDtDZIbANak9lHM3CCXf5kZ1T3bAFv-v8130_assertion type Assertion NP947288.RAkrJB7D1Q2oaDtDZIbANak9lHM3CCXf5kZ1T3bAFv-v8130_head.
- NP947288.RAkrJB7D1Q2oaDtDZIbANak9lHM3CCXf5kZ1T3bAFv-v8130_assertion description "[This case illustrates the clinical heterogeneity that exists in neuropathies associated with MPZ mutations and highlights that in patients with mild hypotonia in the first months that develop a very severe demyelinating neuropathy, the MPZ gene must be taken into account.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP947288.RAkrJB7D1Q2oaDtDZIbANak9lHM3CCXf5kZ1T3bAFv-v8130_provenance.
- NP947288.RAkrJB7D1Q2oaDtDZIbANak9lHM3CCXf5kZ1T3bAFv-v8130_assertion evidence source_evidence_literature NP947288.RAkrJB7D1Q2oaDtDZIbANak9lHM3CCXf5kZ1T3bAFv-v8130_provenance.
- NP947288.RAkrJB7D1Q2oaDtDZIbANak9lHM3CCXf5kZ1T3bAFv-v8130_assertion SIO_000772 22176150 NP947288.RAkrJB7D1Q2oaDtDZIbANak9lHM3CCXf5kZ1T3bAFv-v8130_provenance.
- NP947288.RAkrJB7D1Q2oaDtDZIbANak9lHM3CCXf5kZ1T3bAFv-v8130_assertion wasDerivedFrom befree-2016 NP947288.RAkrJB7D1Q2oaDtDZIbANak9lHM3CCXf5kZ1T3bAFv-v8130_provenance.
- NP947288.RAkrJB7D1Q2oaDtDZIbANak9lHM3CCXf5kZ1T3bAFv-v8130_assertion wasGeneratedBy ECO_0000203 NP947288.RAkrJB7D1Q2oaDtDZIbANak9lHM3CCXf5kZ1T3bAFv-v8130_provenance.