Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP311846.RApmB9EwN79Q_Wyfb4iccTYzuWUimNwY_FMviaHlo4vJY130_assertion> ?p ?o ?g. }
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- NP311846.RApmB9EwN79Q_Wyfb4iccTYzuWUimNwY_FMviaHlo4vJY130_assertion type Assertion NP311846.RApmB9EwN79Q_Wyfb4iccTYzuWUimNwY_FMviaHlo4vJY130_head.
- NP311846.RApmB9EwN79Q_Wyfb4iccTYzuWUimNwY_FMviaHlo4vJY130_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." NP311846.RApmB9EwN79Q_Wyfb4iccTYzuWUimNwY_FMviaHlo4vJY130_provenance.
- NP311846.RApmB9EwN79Q_Wyfb4iccTYzuWUimNwY_FMviaHlo4vJY130_assertion evidence source_evidence_literature NP311846.RApmB9EwN79Q_Wyfb4iccTYzuWUimNwY_FMviaHlo4vJY130_provenance.
- NP311846.RApmB9EwN79Q_Wyfb4iccTYzuWUimNwY_FMviaHlo4vJY130_assertion SIO_000772 16677845 NP311846.RApmB9EwN79Q_Wyfb4iccTYzuWUimNwY_FMviaHlo4vJY130_provenance.
- NP311846.RApmB9EwN79Q_Wyfb4iccTYzuWUimNwY_FMviaHlo4vJY130_assertion wasDerivedFrom befree-20140225 NP311846.RApmB9EwN79Q_Wyfb4iccTYzuWUimNwY_FMviaHlo4vJY130_provenance.
- NP311846.RApmB9EwN79Q_Wyfb4iccTYzuWUimNwY_FMviaHlo4vJY130_assertion wasGeneratedBy ECO_0000203 NP311846.RApmB9EwN79Q_Wyfb4iccTYzuWUimNwY_FMviaHlo4vJY130_provenance.