Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP378015.RAFNqFHHI6QrNUoag37t-nwS6NlS3r139xBRC4X2wuKtg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP378015.RAFNqFHHI6QrNUoag37t-nwS6NlS3r139xBRC4X2wuKtg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP378015.RAFNqFHHI6QrNUoag37t-nwS6NlS3r139xBRC4X2wuKtg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP378015.RAFNqFHHI6QrNUoag37t-nwS6NlS3r139xBRC4X2wuKtg130_provenance.
- NP378015.RAFNqFHHI6QrNUoag37t-nwS6NlS3r139xBRC4X2wuKtg130_assertion description "[The mutilating keratoderma associated with sensorineural hearing loss is thought to have an etiologic basis, resting on a mutation of the GJB2 gene, which encodes the gap junction protein connexin26 (Cx26).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP378015.RAFNqFHHI6QrNUoag37t-nwS6NlS3r139xBRC4X2wuKtg130_provenance.
- NP378015.RAFNqFHHI6QrNUoag37t-nwS6NlS3r139xBRC4X2wuKtg130_assertion evidence source_evidence_literature NP378015.RAFNqFHHI6QrNUoag37t-nwS6NlS3r139xBRC4X2wuKtg130_provenance.
- NP378015.RAFNqFHHI6QrNUoag37t-nwS6NlS3r139xBRC4X2wuKtg130_assertion SIO_000772 11174420 NP378015.RAFNqFHHI6QrNUoag37t-nwS6NlS3r139xBRC4X2wuKtg130_provenance.
- NP378015.RAFNqFHHI6QrNUoag37t-nwS6NlS3r139xBRC4X2wuKtg130_assertion wasDerivedFrom befree-20140225 NP378015.RAFNqFHHI6QrNUoag37t-nwS6NlS3r139xBRC4X2wuKtg130_provenance.
- NP378015.RAFNqFHHI6QrNUoag37t-nwS6NlS3r139xBRC4X2wuKtg130_assertion wasGeneratedBy ECO_0000203 NP378015.RAFNqFHHI6QrNUoag37t-nwS6NlS3r139xBRC4X2wuKtg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP378015.RAFNqFHHI6QrNUoag37t-nwS6NlS3r139xBRC4X2wuKtg130_provenance.