Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP588168.RAoj6QkM62aOU5vfdSUAFdQgfJhvxJg78cVJEkaEuEd5Q130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP588168.RAoj6QkM62aOU5vfdSUAFdQgfJhvxJg78cVJEkaEuEd5Q130_assertion type Assertion NP588168.RAoj6QkM62aOU5vfdSUAFdQgfJhvxJg78cVJEkaEuEd5Q130_head.
- NP588168.RAoj6QkM62aOU5vfdSUAFdQgfJhvxJg78cVJEkaEuEd5Q130_assertion description "[CMT2 is usually inherited as an autosomal dominant trait with a variable age at onset of symptoms associated with progressive axonal neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588168.RAoj6QkM62aOU5vfdSUAFdQgfJhvxJg78cVJEkaEuEd5Q130_provenance.
- NP588168.RAoj6QkM62aOU5vfdSUAFdQgfJhvxJg78cVJEkaEuEd5Q130_assertion evidence source_evidence_literature NP588168.RAoj6QkM62aOU5vfdSUAFdQgfJhvxJg78cVJEkaEuEd5Q130_provenance.
- NP588168.RAoj6QkM62aOU5vfdSUAFdQgfJhvxJg78cVJEkaEuEd5Q130_assertion SIO_000772 7573046 NP588168.RAoj6QkM62aOU5vfdSUAFdQgfJhvxJg78cVJEkaEuEd5Q130_provenance.
- NP588168.RAoj6QkM62aOU5vfdSUAFdQgfJhvxJg78cVJEkaEuEd5Q130_assertion wasDerivedFrom befree-20140225 NP588168.RAoj6QkM62aOU5vfdSUAFdQgfJhvxJg78cVJEkaEuEd5Q130_provenance.
- NP588168.RAoj6QkM62aOU5vfdSUAFdQgfJhvxJg78cVJEkaEuEd5Q130_assertion wasGeneratedBy ECO_0000203 NP588168.RAoj6QkM62aOU5vfdSUAFdQgfJhvxJg78cVJEkaEuEd5Q130_provenance.