Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP352279.RAdwOEEYBHlkVmw4jJ-0NRdvwfQjx0PPyds-YmRiRhm_U130_assertion> ?p ?o ?g. }
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- NP352279.RAdwOEEYBHlkVmw4jJ-0NRdvwfQjx0PPyds-YmRiRhm_U130_assertion type Assertion NP352279.RAdwOEEYBHlkVmw4jJ-0NRdvwfQjx0PPyds-YmRiRhm_U130_head.
- NP352279.RAdwOEEYBHlkVmw4jJ-0NRdvwfQjx0PPyds-YmRiRhm_U130_assertion description "[Three genes responsible for hereditary motor and sensory neuropathy type I (HMSNI) or CMT1 have been identified: peripheral myelin protein 22 (PMP22) and myelin protein zero (MPZ) for the autosomal dominant form and connexin 32 (Cx32) for the X-linked dominant variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP352279.RAdwOEEYBHlkVmw4jJ-0NRdvwfQjx0PPyds-YmRiRhm_U130_provenance.
- NP352279.RAdwOEEYBHlkVmw4jJ-0NRdvwfQjx0PPyds-YmRiRhm_U130_assertion evidence source_evidence_literature NP352279.RAdwOEEYBHlkVmw4jJ-0NRdvwfQjx0PPyds-YmRiRhm_U130_provenance.
- NP352279.RAdwOEEYBHlkVmw4jJ-0NRdvwfQjx0PPyds-YmRiRhm_U130_assertion SIO_000772 10975746 NP352279.RAdwOEEYBHlkVmw4jJ-0NRdvwfQjx0PPyds-YmRiRhm_U130_provenance.
- NP352279.RAdwOEEYBHlkVmw4jJ-0NRdvwfQjx0PPyds-YmRiRhm_U130_assertion wasDerivedFrom befree-20140225 NP352279.RAdwOEEYBHlkVmw4jJ-0NRdvwfQjx0PPyds-YmRiRhm_U130_provenance.
- NP352279.RAdwOEEYBHlkVmw4jJ-0NRdvwfQjx0PPyds-YmRiRhm_U130_assertion wasGeneratedBy ECO_0000203 NP352279.RAdwOEEYBHlkVmw4jJ-0NRdvwfQjx0PPyds-YmRiRhm_U130_provenance.