Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP424688.RAwRO9MKVpwHdF8sfxzZaj9Ns02OeamzmHLhbdef5RIac130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP424688.RAwRO9MKVpwHdF8sfxzZaj9Ns02OeamzmHLhbdef5RIac130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP424688.RAwRO9MKVpwHdF8sfxzZaj9Ns02OeamzmHLhbdef5RIac130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP424688.RAwRO9MKVpwHdF8sfxzZaj9Ns02OeamzmHLhbdef5RIac130_provenance.
- NP424688.RAwRO9MKVpwHdF8sfxzZaj9Ns02OeamzmHLhbdef5RIac130_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." NP424688.RAwRO9MKVpwHdF8sfxzZaj9Ns02OeamzmHLhbdef5RIac130_provenance.
- NP424688.RAwRO9MKVpwHdF8sfxzZaj9Ns02OeamzmHLhbdef5RIac130_assertion evidence source_evidence_literature NP424688.RAwRO9MKVpwHdF8sfxzZaj9Ns02OeamzmHLhbdef5RIac130_provenance.
- NP424688.RAwRO9MKVpwHdF8sfxzZaj9Ns02OeamzmHLhbdef5RIac130_assertion SIO_000772 16677845 NP424688.RAwRO9MKVpwHdF8sfxzZaj9Ns02OeamzmHLhbdef5RIac130_provenance.
- NP424688.RAwRO9MKVpwHdF8sfxzZaj9Ns02OeamzmHLhbdef5RIac130_assertion wasDerivedFrom befree-20140225 NP424688.RAwRO9MKVpwHdF8sfxzZaj9Ns02OeamzmHLhbdef5RIac130_provenance.
- NP424688.RAwRO9MKVpwHdF8sfxzZaj9Ns02OeamzmHLhbdef5RIac130_assertion wasGeneratedBy ECO_0000203 NP424688.RAwRO9MKVpwHdF8sfxzZaj9Ns02OeamzmHLhbdef5RIac130_provenance.
- befree-20140225 importedOn "2014-02-25" NP424688.RAwRO9MKVpwHdF8sfxzZaj9Ns02OeamzmHLhbdef5RIac130_provenance.