Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP598508.RAvCAlnQKWLMYYq1i80n1vy3zgK3-MEKPQMdQBBLx4ZTk130_assertion> ?p ?o ?g. }
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- NP598508.RAvCAlnQKWLMYYq1i80n1vy3zgK3-MEKPQMdQBBLx4ZTk130_assertion type Assertion NP598508.RAvCAlnQKWLMYYq1i80n1vy3zgK3-MEKPQMdQBBLx4ZTk130_head.
- NP598508.RAvCAlnQKWLMYYq1i80n1vy3zgK3-MEKPQMdQBBLx4ZTk130_assertion description "[To investigate the presence of mutations in the parkin gene and the A265G variant in the HS1BP3 gene in a Mexican family with EOPD, ET, and Bell palsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP598508.RAvCAlnQKWLMYYq1i80n1vy3zgK3-MEKPQMdQBBLx4ZTk130_provenance.
- NP598508.RAvCAlnQKWLMYYq1i80n1vy3zgK3-MEKPQMdQBBLx4ZTk130_assertion evidence source_evidence_literature NP598508.RAvCAlnQKWLMYYq1i80n1vy3zgK3-MEKPQMdQBBLx4ZTk130_provenance.
- NP598508.RAvCAlnQKWLMYYq1i80n1vy3zgK3-MEKPQMdQBBLx4ZTk130_assertion SIO_000772 17353387 NP598508.RAvCAlnQKWLMYYq1i80n1vy3zgK3-MEKPQMdQBBLx4ZTk130_provenance.
- NP598508.RAvCAlnQKWLMYYq1i80n1vy3zgK3-MEKPQMdQBBLx4ZTk130_assertion wasDerivedFrom befree-2016 NP598508.RAvCAlnQKWLMYYq1i80n1vy3zgK3-MEKPQMdQBBLx4ZTk130_provenance.
- NP598508.RAvCAlnQKWLMYYq1i80n1vy3zgK3-MEKPQMdQBBLx4ZTk130_assertion wasGeneratedBy ECO_0000203 NP598508.RAvCAlnQKWLMYYq1i80n1vy3zgK3-MEKPQMdQBBLx4ZTk130_provenance.