Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP303856.RAtQhoR47Lr-bhJfU73jZCr-H0VRQ4z5LElsrvgT3bos8130_assertion> ?p ?o ?g. }
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- NP303856.RAtQhoR47Lr-bhJfU73jZCr-H0VRQ4z5LElsrvgT3bos8130_assertion type Assertion NP303856.RAtQhoR47Lr-bhJfU73jZCr-H0VRQ4z5LElsrvgT3bos8130_head.
- NP303856.RAtQhoR47Lr-bhJfU73jZCr-H0VRQ4z5LElsrvgT3bos8130_assertion description "[The peripheral myelin protein 22 mutation W28R was associated with CMT1 and profound deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP303856.RAtQhoR47Lr-bhJfU73jZCr-H0VRQ4z5LElsrvgT3bos8130_provenance.
- NP303856.RAtQhoR47Lr-bhJfU73jZCr-H0VRQ4z5LElsrvgT3bos8130_assertion evidence source_evidence_literature NP303856.RAtQhoR47Lr-bhJfU73jZCr-H0VRQ4z5LElsrvgT3bos8130_provenance.
- NP303856.RAtQhoR47Lr-bhJfU73jZCr-H0VRQ4z5LElsrvgT3bos8130_assertion SIO_000772 11835375 NP303856.RAtQhoR47Lr-bhJfU73jZCr-H0VRQ4z5LElsrvgT3bos8130_provenance.
- NP303856.RAtQhoR47Lr-bhJfU73jZCr-H0VRQ4z5LElsrvgT3bos8130_assertion wasDerivedFrom befree-20140225 NP303856.RAtQhoR47Lr-bhJfU73jZCr-H0VRQ4z5LElsrvgT3bos8130_provenance.
- NP303856.RAtQhoR47Lr-bhJfU73jZCr-H0VRQ4z5LElsrvgT3bos8130_assertion wasGeneratedBy ECO_0000203 NP303856.RAtQhoR47Lr-bhJfU73jZCr-H0VRQ4z5LElsrvgT3bos8130_provenance.