Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP257481.RARuO9luKIdbDnQBFwIJmQm6y-mok7b3uaw8QBT6_uhHg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP257481.RARuO9luKIdbDnQBFwIJmQm6y-mok7b3uaw8QBT6_uhHg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP257481.RARuO9luKIdbDnQBFwIJmQm6y-mok7b3uaw8QBT6_uhHg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP257481.RARuO9luKIdbDnQBFwIJmQm6y-mok7b3uaw8QBT6_uhHg130_provenance.
- NP257481.RARuO9luKIdbDnQBFwIJmQm6y-mok7b3uaw8QBT6_uhHg130_assertion description "[Mutations in connexin26, a cutaneous gap junction protein, cause a wide variety of skin disorders including keratitis-ichthyosis-deafness syndrome (KID).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257481.RARuO9luKIdbDnQBFwIJmQm6y-mok7b3uaw8QBT6_uhHg130_provenance.
- NP257481.RARuO9luKIdbDnQBFwIJmQm6y-mok7b3uaw8QBT6_uhHg130_assertion evidence source_evidence_literature NP257481.RARuO9luKIdbDnQBFwIJmQm6y-mok7b3uaw8QBT6_uhHg130_provenance.
- NP257481.RARuO9luKIdbDnQBFwIJmQm6y-mok7b3uaw8QBT6_uhHg130_assertion SIO_000772 21410767 NP257481.RARuO9luKIdbDnQBFwIJmQm6y-mok7b3uaw8QBT6_uhHg130_provenance.
- NP257481.RARuO9luKIdbDnQBFwIJmQm6y-mok7b3uaw8QBT6_uhHg130_assertion wasDerivedFrom befree-20140225 NP257481.RARuO9luKIdbDnQBFwIJmQm6y-mok7b3uaw8QBT6_uhHg130_provenance.
- NP257481.RARuO9luKIdbDnQBFwIJmQm6y-mok7b3uaw8QBT6_uhHg130_assertion wasGeneratedBy ECO_0000203 NP257481.RARuO9luKIdbDnQBFwIJmQm6y-mok7b3uaw8QBT6_uhHg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP257481.RARuO9luKIdbDnQBFwIJmQm6y-mok7b3uaw8QBT6_uhHg130_provenance.