Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1395619.RAafK48tp5v_x6PvRRMX1dxuiS9gI3RySv4rIvxz1pV9o130_assertion> ?p ?o ?g. }
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- NP1395619.RAafK48tp5v_x6PvRRMX1dxuiS9gI3RySv4rIvxz1pV9o130_assertion type Assertion NP1395619.RAafK48tp5v_x6PvRRMX1dxuiS9gI3RySv4rIvxz1pV9o130_head.
- NP1395619.RAafK48tp5v_x6PvRRMX1dxuiS9gI3RySv4rIvxz1pV9o130_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." NP1395619.RAafK48tp5v_x6PvRRMX1dxuiS9gI3RySv4rIvxz1pV9o130_provenance.
- NP1395619.RAafK48tp5v_x6PvRRMX1dxuiS9gI3RySv4rIvxz1pV9o130_assertion evidence source_evidence_literature NP1395619.RAafK48tp5v_x6PvRRMX1dxuiS9gI3RySv4rIvxz1pV9o130_provenance.
- NP1395619.RAafK48tp5v_x6PvRRMX1dxuiS9gI3RySv4rIvxz1pV9o130_assertion SIO_000772 9595994 NP1395619.RAafK48tp5v_x6PvRRMX1dxuiS9gI3RySv4rIvxz1pV9o130_provenance.
- NP1395619.RAafK48tp5v_x6PvRRMX1dxuiS9gI3RySv4rIvxz1pV9o130_assertion wasDerivedFrom befree-2016 NP1395619.RAafK48tp5v_x6PvRRMX1dxuiS9gI3RySv4rIvxz1pV9o130_provenance.
- NP1395619.RAafK48tp5v_x6PvRRMX1dxuiS9gI3RySv4rIvxz1pV9o130_assertion wasGeneratedBy ECO_0000203 NP1395619.RAafK48tp5v_x6PvRRMX1dxuiS9gI3RySv4rIvxz1pV9o130_provenance.