Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP426330.RA4zVXn-XGgHc6cTKRUo9IhW4dAVd3wTHZE1ZW0O_hNNE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP426330.RA4zVXn-XGgHc6cTKRUo9IhW4dAVd3wTHZE1ZW0O_hNNE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP426330.RA4zVXn-XGgHc6cTKRUo9IhW4dAVd3wTHZE1ZW0O_hNNE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP426330.RA4zVXn-XGgHc6cTKRUo9IhW4dAVd3wTHZE1ZW0O_hNNE130_provenance.
- NP426330.RA4zVXn-XGgHc6cTKRUo9IhW4dAVd3wTHZE1ZW0O_hNNE130_assertion description "[Mutations in connexin 31 (GJB3) and connexin 30.3 (GJB4), implicated in previous reports of EKV, and connexin 26 (GJB2), implicated in palmoplantar keratoderma, were unlikely given the lack of shared homozygous haplotypes in the regions surrounding these genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426330.RA4zVXn-XGgHc6cTKRUo9IhW4dAVd3wTHZE1ZW0O_hNNE130_provenance.
- NP426330.RA4zVXn-XGgHc6cTKRUo9IhW4dAVd3wTHZE1ZW0O_hNNE130_assertion evidence source_evidence_literature NP426330.RA4zVXn-XGgHc6cTKRUo9IhW4dAVd3wTHZE1ZW0O_hNNE130_provenance.
- NP426330.RA4zVXn-XGgHc6cTKRUo9IhW4dAVd3wTHZE1ZW0O_hNNE130_assertion SIO_000772 15668823 NP426330.RA4zVXn-XGgHc6cTKRUo9IhW4dAVd3wTHZE1ZW0O_hNNE130_provenance.
- NP426330.RA4zVXn-XGgHc6cTKRUo9IhW4dAVd3wTHZE1ZW0O_hNNE130_assertion wasDerivedFrom befree-20150227 NP426330.RA4zVXn-XGgHc6cTKRUo9IhW4dAVd3wTHZE1ZW0O_hNNE130_provenance.
- NP426330.RA4zVXn-XGgHc6cTKRUo9IhW4dAVd3wTHZE1ZW0O_hNNE130_assertion wasGeneratedBy ECO_0000203 NP426330.RA4zVXn-XGgHc6cTKRUo9IhW4dAVd3wTHZE1ZW0O_hNNE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP426330.RA4zVXn-XGgHc6cTKRUo9IhW4dAVd3wTHZE1ZW0O_hNNE130_provenance.