Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1276202.RAs9SN1kzOvSM6fG-9x-qNTQ5pylkvlogiaz9w1rLbjpc130_assertion> ?p ?o ?g. }
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- NP1276202.RAs9SN1kzOvSM6fG-9x-qNTQ5pylkvlogiaz9w1rLbjpc130_assertion type Assertion NP1276202.RAs9SN1kzOvSM6fG-9x-qNTQ5pylkvlogiaz9w1rLbjpc130_head.
- NP1276202.RAs9SN1kzOvSM6fG-9x-qNTQ5pylkvlogiaz9w1rLbjpc130_assertion description "[GDAP1 mutations also alter fission, fusion and transport of mitochondria and are associated either with recessive demyelinating (CMT4A) and axonal CMT (AR-CMT2K) and, less commonly, with dominant, milder, axonal CMT (CMT2K).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1276202.RAs9SN1kzOvSM6fG-9x-qNTQ5pylkvlogiaz9w1rLbjpc130_provenance.
- NP1276202.RAs9SN1kzOvSM6fG-9x-qNTQ5pylkvlogiaz9w1rLbjpc130_assertion evidence source_evidence_literature NP1276202.RAs9SN1kzOvSM6fG-9x-qNTQ5pylkvlogiaz9w1rLbjpc130_provenance.
- NP1276202.RAs9SN1kzOvSM6fG-9x-qNTQ5pylkvlogiaz9w1rLbjpc130_assertion SIO_000772 25847151 NP1276202.RAs9SN1kzOvSM6fG-9x-qNTQ5pylkvlogiaz9w1rLbjpc130_provenance.
- NP1276202.RAs9SN1kzOvSM6fG-9x-qNTQ5pylkvlogiaz9w1rLbjpc130_assertion wasDerivedFrom befree-2016 NP1276202.RAs9SN1kzOvSM6fG-9x-qNTQ5pylkvlogiaz9w1rLbjpc130_provenance.
- NP1276202.RAs9SN1kzOvSM6fG-9x-qNTQ5pylkvlogiaz9w1rLbjpc130_assertion wasGeneratedBy ECO_0000203 NP1276202.RAs9SN1kzOvSM6fG-9x-qNTQ5pylkvlogiaz9w1rLbjpc130_provenance.