Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP944627.RA3CwQti1wtTQsICVezEjI7bo9qBZwXthUHfTkBFVIcsI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP944627.RA3CwQti1wtTQsICVezEjI7bo9qBZwXthUHfTkBFVIcsI130_assertion type Assertion NP944627.RA3CwQti1wtTQsICVezEjI7bo9qBZwXthUHfTkBFVIcsI130_head.
- NP944627.RA3CwQti1wtTQsICVezEjI7bo9qBZwXthUHfTkBFVIcsI130_assertion description "[Mutations in the SH3TC2 gene are a frequent cause of demyelinating hereditary neuropathy among Czech patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP944627.RA3CwQti1wtTQsICVezEjI7bo9qBZwXthUHfTkBFVIcsI130_provenance.
- NP944627.RA3CwQti1wtTQsICVezEjI7bo9qBZwXthUHfTkBFVIcsI130_assertion evidence source_evidence_literature NP944627.RA3CwQti1wtTQsICVezEjI7bo9qBZwXthUHfTkBFVIcsI130_provenance.
- NP944627.RA3CwQti1wtTQsICVezEjI7bo9qBZwXthUHfTkBFVIcsI130_assertion SIO_000772 21291453 NP944627.RA3CwQti1wtTQsICVezEjI7bo9qBZwXthUHfTkBFVIcsI130_provenance.
- NP944627.RA3CwQti1wtTQsICVezEjI7bo9qBZwXthUHfTkBFVIcsI130_assertion wasDerivedFrom befree-20150227 NP944627.RA3CwQti1wtTQsICVezEjI7bo9qBZwXthUHfTkBFVIcsI130_provenance.
- NP944627.RA3CwQti1wtTQsICVezEjI7bo9qBZwXthUHfTkBFVIcsI130_assertion wasGeneratedBy ECO_0000203 NP944627.RA3CwQti1wtTQsICVezEjI7bo9qBZwXthUHfTkBFVIcsI130_provenance.