Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP699761.RA6pcjfGjAAUA1ghKabZ5eOQFoUBbqByql-MQqe8QQml0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP699761.RA6pcjfGjAAUA1ghKabZ5eOQFoUBbqByql-MQqe8QQml0130_assertion type Assertion NP699761.RA6pcjfGjAAUA1ghKabZ5eOQFoUBbqByql-MQqe8QQml0130_head.
- NP699761.RA6pcjfGjAAUA1ghKabZ5eOQFoUBbqByql-MQqe8QQml0130_assertion wasGeneratedBy ECO_0000203 NP699761.RA6pcjfGjAAUA1ghKabZ5eOQFoUBbqByql-MQqe8QQml0130_provenance.
- NP699761.RA6pcjfGjAAUA1ghKabZ5eOQFoUBbqByql-MQqe8QQml0130_assertion wasDerivedFrom befree-2016 NP699761.RA6pcjfGjAAUA1ghKabZ5eOQFoUBbqByql-MQqe8QQml0130_provenance.
- NP699761.RA6pcjfGjAAUA1ghKabZ5eOQFoUBbqByql-MQqe8QQml0130_assertion SIO_000772 18950394 NP699761.RA6pcjfGjAAUA1ghKabZ5eOQFoUBbqByql-MQqe8QQml0130_provenance.
- NP699761.RA6pcjfGjAAUA1ghKabZ5eOQFoUBbqByql-MQqe8QQml0130_assertion evidence source_evidence_literature NP699761.RA6pcjfGjAAUA1ghKabZ5eOQFoUBbqByql-MQqe8QQml0130_provenance.
- NP699761.RA6pcjfGjAAUA1ghKabZ5eOQFoUBbqByql-MQqe8QQml0130_assertion description "[A report of GJB2 (N14K) Connexin 26 mutation in two patients--a new subtype of KID syndrome?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP699761.RA6pcjfGjAAUA1ghKabZ5eOQFoUBbqByql-MQqe8QQml0130_provenance.