Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP583002.RAzEhSV9X4THe7G1DyPmsIxl4jRjxDPZuEBd9jpKEBKbU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP583002.RAzEhSV9X4THe7G1DyPmsIxl4jRjxDPZuEBd9jpKEBKbU130_assertion type Assertion NP583002.RAzEhSV9X4THe7G1DyPmsIxl4jRjxDPZuEBd9jpKEBKbU130_head.
- NP583002.RAzEhSV9X4THe7G1DyPmsIxl4jRjxDPZuEBd9jpKEBKbU130_assertion description "[In the field of the peripheral neuropathies we present data on a newly described autosomal recessive Charcot-Marie-Tooth disease (CMT4F) with mutations in the periaxin gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583002.RAzEhSV9X4THe7G1DyPmsIxl4jRjxDPZuEBd9jpKEBKbU130_provenance.
- NP583002.RAzEhSV9X4THe7G1DyPmsIxl4jRjxDPZuEBd9jpKEBKbU130_assertion evidence source_evidence_literature NP583002.RAzEhSV9X4THe7G1DyPmsIxl4jRjxDPZuEBd9jpKEBKbU130_provenance.
- NP583002.RAzEhSV9X4THe7G1DyPmsIxl4jRjxDPZuEBd9jpKEBKbU130_assertion SIO_000772 12094560 NP583002.RAzEhSV9X4THe7G1DyPmsIxl4jRjxDPZuEBd9jpKEBKbU130_provenance.
- NP583002.RAzEhSV9X4THe7G1DyPmsIxl4jRjxDPZuEBd9jpKEBKbU130_assertion wasDerivedFrom befree-20140225 NP583002.RAzEhSV9X4THe7G1DyPmsIxl4jRjxDPZuEBd9jpKEBKbU130_provenance.
- NP583002.RAzEhSV9X4THe7G1DyPmsIxl4jRjxDPZuEBd9jpKEBKbU130_assertion wasGeneratedBy ECO_0000203 NP583002.RAzEhSV9X4THe7G1DyPmsIxl4jRjxDPZuEBd9jpKEBKbU130_provenance.