Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP180274.RAzStlgvkXo56KwxvYmdL9VWvEBMI3Vi39eQr3EYnr-Fo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP180274.RAzStlgvkXo56KwxvYmdL9VWvEBMI3Vi39eQr3EYnr-Fo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP180274.RAzStlgvkXo56KwxvYmdL9VWvEBMI3Vi39eQr3EYnr-Fo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP180274.RAzStlgvkXo56KwxvYmdL9VWvEBMI3Vi39eQr3EYnr-Fo130_provenance.
- NP180274.RAzStlgvkXo56KwxvYmdL9VWvEBMI3Vi39eQr3EYnr-Fo130_assertion description "[Prospective variants screening of connexin genes in children with hearing impairment: genotype/phenotype correlation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP180274.RAzStlgvkXo56KwxvYmdL9VWvEBMI3Vi39eQr3EYnr-Fo130_provenance.
- NP180274.RAzStlgvkXo56KwxvYmdL9VWvEBMI3Vi39eQr3EYnr-Fo130_assertion evidence source_evidence_literature NP180274.RAzStlgvkXo56KwxvYmdL9VWvEBMI3Vi39eQr3EYnr-Fo130_provenance.
- NP180274.RAzStlgvkXo56KwxvYmdL9VWvEBMI3Vi39eQr3EYnr-Fo130_assertion SIO_000772 20593197 NP180274.RAzStlgvkXo56KwxvYmdL9VWvEBMI3Vi39eQr3EYnr-Fo130_provenance.
- NP180274.RAzStlgvkXo56KwxvYmdL9VWvEBMI3Vi39eQr3EYnr-Fo130_assertion wasDerivedFrom gad-20150221 NP180274.RAzStlgvkXo56KwxvYmdL9VWvEBMI3Vi39eQr3EYnr-Fo130_provenance.
- NP180274.RAzStlgvkXo56KwxvYmdL9VWvEBMI3Vi39eQr3EYnr-Fo130_assertion wasGeneratedBy ECO_0000203 NP180274.RAzStlgvkXo56KwxvYmdL9VWvEBMI3Vi39eQr3EYnr-Fo130_provenance.
- gad-20150221 importedOn "2015-02-21" NP180274.RAzStlgvkXo56KwxvYmdL9VWvEBMI3Vi39eQr3EYnr-Fo130_provenance.