Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP344403.RASt7Lvo8P6LhzFcZYD_6htIVZQ-zTD_mKzYDYqI3C27c130_assertion> ?p ?o ?g. }
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- NP344403.RASt7Lvo8P6LhzFcZYD_6htIVZQ-zTD_mKzYDYqI3C27c130_assertion type Assertion NP344403.RASt7Lvo8P6LhzFcZYD_6htIVZQ-zTD_mKzYDYqI3C27c130_head.
- NP344403.RASt7Lvo8P6LhzFcZYD_6htIVZQ-zTD_mKzYDYqI3C27c130_assertion description "[In the process of screening the above cohort of patients as well as other patients for CMT-causative mutations, we identified several previously unreported mutant alleles: two for connexin 32, three for myelin protein zero, and two for peripheral myelin protein 22.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP344403.RASt7Lvo8P6LhzFcZYD_6htIVZQ-zTD_mKzYDYqI3C27c130_provenance.
- NP344403.RASt7Lvo8P6LhzFcZYD_6htIVZQ-zTD_mKzYDYqI3C27c130_assertion evidence source_evidence_literature NP344403.RASt7Lvo8P6LhzFcZYD_6htIVZQ-zTD_mKzYDYqI3C27c130_provenance.
- NP344403.RASt7Lvo8P6LhzFcZYD_6htIVZQ-zTD_mKzYDYqI3C27c130_assertion SIO_000772 11835375 NP344403.RASt7Lvo8P6LhzFcZYD_6htIVZQ-zTD_mKzYDYqI3C27c130_provenance.
- NP344403.RASt7Lvo8P6LhzFcZYD_6htIVZQ-zTD_mKzYDYqI3C27c130_assertion wasDerivedFrom befree-2016 NP344403.RASt7Lvo8P6LhzFcZYD_6htIVZQ-zTD_mKzYDYqI3C27c130_provenance.
- NP344403.RASt7Lvo8P6LhzFcZYD_6htIVZQ-zTD_mKzYDYqI3C27c130_assertion wasGeneratedBy ECO_0000203 NP344403.RASt7Lvo8P6LhzFcZYD_6htIVZQ-zTD_mKzYDYqI3C27c130_provenance.