Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1186886.RAIKPJdazaBdHmYpKBCH2c0bejBxul00vdiROX7xQydAE130_assertion> ?p ?o ?g. }
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- NP1186886.RAIKPJdazaBdHmYpKBCH2c0bejBxul00vdiROX7xQydAE130_assertion type Assertion NP1186886.RAIKPJdazaBdHmYpKBCH2c0bejBxul00vdiROX7xQydAE130_head.
- NP1186886.RAIKPJdazaBdHmYpKBCH2c0bejBxul00vdiROX7xQydAE130_assertion description "[Disorders with a known molecular basis falling within this group include hereditary neuropathy with liability to pressure palsies (HNPP) due to the deletion of the PMP22 gene or to mutations in this same gene, and hereditary neuralgic amyotrophy (HNA) caused by mutations in the SEPT9 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1186886.RAIKPJdazaBdHmYpKBCH2c0bejBxul00vdiROX7xQydAE130_provenance.
- NP1186886.RAIKPJdazaBdHmYpKBCH2c0bejBxul00vdiROX7xQydAE130_assertion evidence source_evidence_literature NP1186886.RAIKPJdazaBdHmYpKBCH2c0bejBxul00vdiROX7xQydAE130_provenance.
- NP1186886.RAIKPJdazaBdHmYpKBCH2c0bejBxul00vdiROX7xQydAE130_assertion SIO_000772 24878226 NP1186886.RAIKPJdazaBdHmYpKBCH2c0bejBxul00vdiROX7xQydAE130_provenance.
- NP1186886.RAIKPJdazaBdHmYpKBCH2c0bejBxul00vdiROX7xQydAE130_assertion wasDerivedFrom befree-2016 NP1186886.RAIKPJdazaBdHmYpKBCH2c0bejBxul00vdiROX7xQydAE130_provenance.
- NP1186886.RAIKPJdazaBdHmYpKBCH2c0bejBxul00vdiROX7xQydAE130_assertion wasGeneratedBy ECO_0000203 NP1186886.RAIKPJdazaBdHmYpKBCH2c0bejBxul00vdiROX7xQydAE130_provenance.