Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP905617.RAAhRsvcN6bkrEl1DO5KNCiYZ4Z9C85lRKn4gqkVJQQOw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP905617.RAAhRsvcN6bkrEl1DO5KNCiYZ4Z9C85lRKn4gqkVJQQOw130_assertion type Assertion NP905617.RAAhRsvcN6bkrEl1DO5KNCiYZ4Z9C85lRKn4gqkVJQQOw130_head.
- NP905617.RAAhRsvcN6bkrEl1DO5KNCiYZ4Z9C85lRKn4gqkVJQQOw130_assertion description "[ACTA2 mutations were identified in 16% of a cohort presenting familial TAAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP905617.RAAhRsvcN6bkrEl1DO5KNCiYZ4Z9C85lRKn4gqkVJQQOw130_provenance.
- NP905617.RAAhRsvcN6bkrEl1DO5KNCiYZ4Z9C85lRKn4gqkVJQQOw130_assertion evidence source_evidence_literature NP905617.RAAhRsvcN6bkrEl1DO5KNCiYZ4Z9C85lRKn4gqkVJQQOw130_provenance.
- NP905617.RAAhRsvcN6bkrEl1DO5KNCiYZ4Z9C85lRKn4gqkVJQQOw130_assertion SIO_000772 21937134 NP905617.RAAhRsvcN6bkrEl1DO5KNCiYZ4Z9C85lRKn4gqkVJQQOw130_provenance.
- NP905617.RAAhRsvcN6bkrEl1DO5KNCiYZ4Z9C85lRKn4gqkVJQQOw130_assertion wasDerivedFrom befree-20140225 NP905617.RAAhRsvcN6bkrEl1DO5KNCiYZ4Z9C85lRKn4gqkVJQQOw130_provenance.
- NP905617.RAAhRsvcN6bkrEl1DO5KNCiYZ4Z9C85lRKn4gqkVJQQOw130_assertion wasGeneratedBy ECO_0000203 NP905617.RAAhRsvcN6bkrEl1DO5KNCiYZ4Z9C85lRKn4gqkVJQQOw130_provenance.