Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP746734.RALGO3cIOcRWOU0fydmkulwIdG6rpSVa8KftRYQgMFfJg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP746734.RALGO3cIOcRWOU0fydmkulwIdG6rpSVa8KftRYQgMFfJg130_assertion type Assertion NP746734.RALGO3cIOcRWOU0fydmkulwIdG6rpSVa8KftRYQgMFfJg130_head.
- NP746734.RALGO3cIOcRWOU0fydmkulwIdG6rpSVa8KftRYQgMFfJg130_assertion description "[Interestingly, mutations of connexin genes have been reported in several human diseases (peripheral neuropathies, cardiovascular and dermatological diseases, hereditary cataract, and deafness) and altered expression of connexins have been associated with tumoral progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP746734.RALGO3cIOcRWOU0fydmkulwIdG6rpSVa8KftRYQgMFfJg130_provenance.
- NP746734.RALGO3cIOcRWOU0fydmkulwIdG6rpSVa8KftRYQgMFfJg130_assertion evidence source_evidence_literature NP746734.RALGO3cIOcRWOU0fydmkulwIdG6rpSVa8KftRYQgMFfJg130_provenance.
- NP746734.RALGO3cIOcRWOU0fydmkulwIdG6rpSVa8KftRYQgMFfJg130_assertion SIO_000772 16677845 NP746734.RALGO3cIOcRWOU0fydmkulwIdG6rpSVa8KftRYQgMFfJg130_provenance.
- NP746734.RALGO3cIOcRWOU0fydmkulwIdG6rpSVa8KftRYQgMFfJg130_assertion wasDerivedFrom befree-20140225 NP746734.RALGO3cIOcRWOU0fydmkulwIdG6rpSVa8KftRYQgMFfJg130_provenance.
- NP746734.RALGO3cIOcRWOU0fydmkulwIdG6rpSVa8KftRYQgMFfJg130_assertion wasGeneratedBy ECO_0000203 NP746734.RALGO3cIOcRWOU0fydmkulwIdG6rpSVa8KftRYQgMFfJg130_provenance.