Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP968744.RAGqoOv2p6Gi6Cz3hp1U26uFwoWwjkWsJQ0FbgYZNmRkA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP968744.RAGqoOv2p6Gi6Cz3hp1U26uFwoWwjkWsJQ0FbgYZNmRkA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP968744.RAGqoOv2p6Gi6Cz3hp1U26uFwoWwjkWsJQ0FbgYZNmRkA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP968744.RAGqoOv2p6Gi6Cz3hp1U26uFwoWwjkWsJQ0FbgYZNmRkA130_provenance.
- NP968744.RAGqoOv2p6Gi6Cz3hp1U26uFwoWwjkWsJQ0FbgYZNmRkA130_assertion description "[We recently identified mutations in either GJB3 or GJB4 genes, encoding respectively connexin 31 (Cx31) or 30.3 (Cx30.3), as causally involved in erythrokeratodermia variabilis (EKV), a mostly autosomal dominant disorder of keratinization.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP968744.RAGqoOv2p6Gi6Cz3hp1U26uFwoWwjkWsJQ0FbgYZNmRkA130_provenance.
- NP968744.RAGqoOv2p6Gi6Cz3hp1U26uFwoWwjkWsJQ0FbgYZNmRkA130_assertion evidence source_evidence_literature NP968744.RAGqoOv2p6Gi6Cz3hp1U26uFwoWwjkWsJQ0FbgYZNmRkA130_provenance.
- NP968744.RAGqoOv2p6Gi6Cz3hp1U26uFwoWwjkWsJQ0FbgYZNmRkA130_assertion SIO_000772 14583444 NP968744.RAGqoOv2p6Gi6Cz3hp1U26uFwoWwjkWsJQ0FbgYZNmRkA130_provenance.
- NP968744.RAGqoOv2p6Gi6Cz3hp1U26uFwoWwjkWsJQ0FbgYZNmRkA130_assertion wasDerivedFrom befree-20150227 NP968744.RAGqoOv2p6Gi6Cz3hp1U26uFwoWwjkWsJQ0FbgYZNmRkA130_provenance.
- NP968744.RAGqoOv2p6Gi6Cz3hp1U26uFwoWwjkWsJQ0FbgYZNmRkA130_assertion wasGeneratedBy ECO_0000203 NP968744.RAGqoOv2p6Gi6Cz3hp1U26uFwoWwjkWsJQ0FbgYZNmRkA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP968744.RAGqoOv2p6Gi6Cz3hp1U26uFwoWwjkWsJQ0FbgYZNmRkA130_provenance.