Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1367752.RAaqsRpNbhaZ9_KLJ_q-G6gyNkU8XhGbJw_HWKEcktf84130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1367752.RAaqsRpNbhaZ9_KLJ_q-G6gyNkU8XhGbJw_HWKEcktf84130_assertion type Assertion NP1367752.RAaqsRpNbhaZ9_KLJ_q-G6gyNkU8XhGbJw_HWKEcktf84130_head.
- NP1367752.RAaqsRpNbhaZ9_KLJ_q-G6gyNkU8XhGbJw_HWKEcktf84130_assertion description "[A novel frameshift mutation in PMP22 accounts for hereditary neuropathy with liability to pressure palsies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1367752.RAaqsRpNbhaZ9_KLJ_q-G6gyNkU8XhGbJw_HWKEcktf84130_provenance.
- NP1367752.RAaqsRpNbhaZ9_KLJ_q-G6gyNkU8XhGbJw_HWKEcktf84130_assertion evidence source_evidence_literature NP1367752.RAaqsRpNbhaZ9_KLJ_q-G6gyNkU8XhGbJw_HWKEcktf84130_provenance.
- NP1367752.RAaqsRpNbhaZ9_KLJ_q-G6gyNkU8XhGbJw_HWKEcktf84130_assertion SIO_000772 9040737 NP1367752.RAaqsRpNbhaZ9_KLJ_q-G6gyNkU8XhGbJw_HWKEcktf84130_provenance.
- NP1367752.RAaqsRpNbhaZ9_KLJ_q-G6gyNkU8XhGbJw_HWKEcktf84130_assertion wasDerivedFrom befree-2016 NP1367752.RAaqsRpNbhaZ9_KLJ_q-G6gyNkU8XhGbJw_HWKEcktf84130_provenance.
- NP1367752.RAaqsRpNbhaZ9_KLJ_q-G6gyNkU8XhGbJw_HWKEcktf84130_assertion wasGeneratedBy ECO_0000203 NP1367752.RAaqsRpNbhaZ9_KLJ_q-G6gyNkU8XhGbJw_HWKEcktf84130_provenance.