Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1012208.RAD7HAtGBhSzRTptra1DTENkbvQPriKZUy4AK7y_GZOIA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1012208.RAD7HAtGBhSzRTptra1DTENkbvQPriKZUy4AK7y_GZOIA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1012208.RAD7HAtGBhSzRTptra1DTENkbvQPriKZUy4AK7y_GZOIA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1012208.RAD7HAtGBhSzRTptra1DTENkbvQPriKZUy4AK7y_GZOIA130_provenance.
- NP1012208.RAD7HAtGBhSzRTptra1DTENkbvQPriKZUy4AK7y_GZOIA130_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." NP1012208.RAD7HAtGBhSzRTptra1DTENkbvQPriKZUy4AK7y_GZOIA130_provenance.
- NP1012208.RAD7HAtGBhSzRTptra1DTENkbvQPriKZUy4AK7y_GZOIA130_assertion evidence source_evidence_literature NP1012208.RAD7HAtGBhSzRTptra1DTENkbvQPriKZUy4AK7y_GZOIA130_provenance.
- NP1012208.RAD7HAtGBhSzRTptra1DTENkbvQPriKZUy4AK7y_GZOIA130_assertion SIO_000772 16677845 NP1012208.RAD7HAtGBhSzRTptra1DTENkbvQPriKZUy4AK7y_GZOIA130_provenance.
- NP1012208.RAD7HAtGBhSzRTptra1DTENkbvQPriKZUy4AK7y_GZOIA130_assertion wasDerivedFrom befree-20150227 NP1012208.RAD7HAtGBhSzRTptra1DTENkbvQPriKZUy4AK7y_GZOIA130_provenance.
- NP1012208.RAD7HAtGBhSzRTptra1DTENkbvQPriKZUy4AK7y_GZOIA130_assertion wasGeneratedBy ECO_0000203 NP1012208.RAD7HAtGBhSzRTptra1DTENkbvQPriKZUy4AK7y_GZOIA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1012208.RAD7HAtGBhSzRTptra1DTENkbvQPriKZUy4AK7y_GZOIA130_provenance.