Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP513298.RAjjI7yIQ_eQ-iT5i6ePbRoit73mJElWSV5WLEckYoW3Q130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP513298.RAjjI7yIQ_eQ-iT5i6ePbRoit73mJElWSV5WLEckYoW3Q130_assertion type Assertion NP513298.RAjjI7yIQ_eQ-iT5i6ePbRoit73mJElWSV5WLEckYoW3Q130_head.
- NP513298.RAjjI7yIQ_eQ-iT5i6ePbRoit73mJElWSV5WLEckYoW3Q130_assertion description "[Mutations of the myelin protein zero (MPZ) gene have been associated with CMT1B, Dejerine-Sottas disease, and congenital hypomyelination, which are inherited demyelinating neuropathies characterized by different clinical severity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP513298.RAjjI7yIQ_eQ-iT5i6ePbRoit73mJElWSV5WLEckYoW3Q130_provenance.
- NP513298.RAjjI7yIQ_eQ-iT5i6ePbRoit73mJElWSV5WLEckYoW3Q130_assertion evidence source_evidence_literature NP513298.RAjjI7yIQ_eQ-iT5i6ePbRoit73mJElWSV5WLEckYoW3Q130_provenance.
- NP513298.RAjjI7yIQ_eQ-iT5i6ePbRoit73mJElWSV5WLEckYoW3Q130_assertion SIO_000772 9595994 NP513298.RAjjI7yIQ_eQ-iT5i6ePbRoit73mJElWSV5WLEckYoW3Q130_provenance.
- NP513298.RAjjI7yIQ_eQ-iT5i6ePbRoit73mJElWSV5WLEckYoW3Q130_assertion wasDerivedFrom befree-20140225 NP513298.RAjjI7yIQ_eQ-iT5i6ePbRoit73mJElWSV5WLEckYoW3Q130_provenance.
- NP513298.RAjjI7yIQ_eQ-iT5i6ePbRoit73mJElWSV5WLEckYoW3Q130_assertion wasGeneratedBy ECO_0000203 NP513298.RAjjI7yIQ_eQ-iT5i6ePbRoit73mJElWSV5WLEckYoW3Q130_provenance.