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- NP662290.RAyC5OXQYIALkCpWBxo5o3PcLzDeR-d4zDP3eHEuNVTTs130_assertion type Assertion NP662290.RAyC5OXQYIALkCpWBxo5o3PcLzDeR-d4zDP3eHEuNVTTs130_head.
- NP662290.RAyC5OXQYIALkCpWBxo5o3PcLzDeR-d4zDP3eHEuNVTTs130_assertion wasGeneratedBy ECO_0000203 NP662290.RAyC5OXQYIALkCpWBxo5o3PcLzDeR-d4zDP3eHEuNVTTs130_provenance.
- NP662290.RAyC5OXQYIALkCpWBxo5o3PcLzDeR-d4zDP3eHEuNVTTs130_assertion wasDerivedFrom befree-20150227 NP662290.RAyC5OXQYIALkCpWBxo5o3PcLzDeR-d4zDP3eHEuNVTTs130_provenance.
- NP662290.RAyC5OXQYIALkCpWBxo5o3PcLzDeR-d4zDP3eHEuNVTTs130_assertion SIO_000772 11535114 NP662290.RAyC5OXQYIALkCpWBxo5o3PcLzDeR-d4zDP3eHEuNVTTs130_provenance.
- NP662290.RAyC5OXQYIALkCpWBxo5o3PcLzDeR-d4zDP3eHEuNVTTs130_assertion evidence source_evidence_literature NP662290.RAyC5OXQYIALkCpWBxo5o3PcLzDeR-d4zDP3eHEuNVTTs130_provenance.
- NP662290.RAyC5OXQYIALkCpWBxo5o3PcLzDeR-d4zDP3eHEuNVTTs130_assertion description "[Similarities are drawn with the peripheral neuropathies Charcot-Marie-Tooth disease Type 1 (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP) that are also caused by dosage effects and mutations in a single myelin protein gene (peripheral myelin protein 22, PMP-22).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP662290.RAyC5OXQYIALkCpWBxo5o3PcLzDeR-d4zDP3eHEuNVTTs130_provenance.