Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP548389.RAQHJJLkn55u5yGms1eQA8RZn1tZ0YCZMekhxsUiZ9lfA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP548389.RAQHJJLkn55u5yGms1eQA8RZn1tZ0YCZMekhxsUiZ9lfA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP548389.RAQHJJLkn55u5yGms1eQA8RZn1tZ0YCZMekhxsUiZ9lfA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP548389.RAQHJJLkn55u5yGms1eQA8RZn1tZ0YCZMekhxsUiZ9lfA130_provenance.
- NP548389.RAQHJJLkn55u5yGms1eQA8RZn1tZ0YCZMekhxsUiZ9lfA130_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." NP548389.RAQHJJLkn55u5yGms1eQA8RZn1tZ0YCZMekhxsUiZ9lfA130_provenance.
- NP548389.RAQHJJLkn55u5yGms1eQA8RZn1tZ0YCZMekhxsUiZ9lfA130_assertion evidence source_evidence_literature NP548389.RAQHJJLkn55u5yGms1eQA8RZn1tZ0YCZMekhxsUiZ9lfA130_provenance.
- NP548389.RAQHJJLkn55u5yGms1eQA8RZn1tZ0YCZMekhxsUiZ9lfA130_assertion SIO_000772 16677845 NP548389.RAQHJJLkn55u5yGms1eQA8RZn1tZ0YCZMekhxsUiZ9lfA130_provenance.
- NP548389.RAQHJJLkn55u5yGms1eQA8RZn1tZ0YCZMekhxsUiZ9lfA130_assertion wasDerivedFrom befree-2016 NP548389.RAQHJJLkn55u5yGms1eQA8RZn1tZ0YCZMekhxsUiZ9lfA130_provenance.
- NP548389.RAQHJJLkn55u5yGms1eQA8RZn1tZ0YCZMekhxsUiZ9lfA130_assertion wasGeneratedBy ECO_0000203 NP548389.RAQHJJLkn55u5yGms1eQA8RZn1tZ0YCZMekhxsUiZ9lfA130_provenance.
- befree-2016 importedOn "2016-02-19" NP548389.RAQHJJLkn55u5yGms1eQA8RZn1tZ0YCZMekhxsUiZ9lfA130_provenance.