Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP663082.RAXngu1eT65B7HkwwWt3vHYu7nzOMws-d0eXnvNew83ZQ130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP663082.RAXngu1eT65B7HkwwWt3vHYu7nzOMws-d0eXnvNew83ZQ130_assertion type Assertion NP663082.RAXngu1eT65B7HkwwWt3vHYu7nzOMws-d0eXnvNew83ZQ130_head.
- NP663082.RAXngu1eT65B7HkwwWt3vHYu7nzOMws-d0eXnvNew83ZQ130_assertion description "[Thus, SBMA is the first genetic disease in which a strong correlation between the degree of genetic abnormality (number of CAG tandem repeats) and clinical phenotypic expression is demonstrable.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP663082.RAXngu1eT65B7HkwwWt3vHYu7nzOMws-d0eXnvNew83ZQ130_provenance.
- NP663082.RAXngu1eT65B7HkwwWt3vHYu7nzOMws-d0eXnvNew83ZQ130_assertion evidence source_evidence_literature NP663082.RAXngu1eT65B7HkwwWt3vHYu7nzOMws-d0eXnvNew83ZQ130_provenance.
- NP663082.RAXngu1eT65B7HkwwWt3vHYu7nzOMws-d0eXnvNew83ZQ130_assertion SIO_000772 1461383 NP663082.RAXngu1eT65B7HkwwWt3vHYu7nzOMws-d0eXnvNew83ZQ130_provenance.
- NP663082.RAXngu1eT65B7HkwwWt3vHYu7nzOMws-d0eXnvNew83ZQ130_assertion wasDerivedFrom befree-20140225 NP663082.RAXngu1eT65B7HkwwWt3vHYu7nzOMws-d0eXnvNew83ZQ130_provenance.
- NP663082.RAXngu1eT65B7HkwwWt3vHYu7nzOMws-d0eXnvNew83ZQ130_assertion wasGeneratedBy ECO_0000203 NP663082.RAXngu1eT65B7HkwwWt3vHYu7nzOMws-d0eXnvNew83ZQ130_provenance.