Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP745025.RAFSzOcndEWmX_YOb4wkqiD-U86_WHNAvbPw4Q1Sqw7VA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP745025.RAFSzOcndEWmX_YOb4wkqiD-U86_WHNAvbPw4Q1Sqw7VA130_assertion type Assertion NP745025.RAFSzOcndEWmX_YOb4wkqiD-U86_WHNAvbPw4Q1Sqw7VA130_head.
- NP745025.RAFSzOcndEWmX_YOb4wkqiD-U86_WHNAvbPw4Q1Sqw7VA130_assertion description "[Many of the mutations known to cause either syndromic or nonsyndromic deafness occur in genes that interact with actin (e.g., the myosins, espin, and harmonin).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP745025.RAFSzOcndEWmX_YOb4wkqiD-U86_WHNAvbPw4Q1Sqw7VA130_provenance.
- NP745025.RAFSzOcndEWmX_YOb4wkqiD-U86_WHNAvbPw4Q1Sqw7VA130_assertion evidence source_evidence_literature NP745025.RAFSzOcndEWmX_YOb4wkqiD-U86_WHNAvbPw4Q1Sqw7VA130_provenance.
- NP745025.RAFSzOcndEWmX_YOb4wkqiD-U86_WHNAvbPw4Q1Sqw7VA130_assertion SIO_000772 13680526 NP745025.RAFSzOcndEWmX_YOb4wkqiD-U86_WHNAvbPw4Q1Sqw7VA130_provenance.
- NP745025.RAFSzOcndEWmX_YOb4wkqiD-U86_WHNAvbPw4Q1Sqw7VA130_assertion wasDerivedFrom befree-20140225 NP745025.RAFSzOcndEWmX_YOb4wkqiD-U86_WHNAvbPw4Q1Sqw7VA130_provenance.
- NP745025.RAFSzOcndEWmX_YOb4wkqiD-U86_WHNAvbPw4Q1Sqw7VA130_assertion wasGeneratedBy ECO_0000203 NP745025.RAFSzOcndEWmX_YOb4wkqiD-U86_WHNAvbPw4Q1Sqw7VA130_provenance.