Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP378015.RAFNqFHHI6QrNUoag37t-nwS6NlS3r139xBRC4X2wuKtg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP378015.RAFNqFHHI6QrNUoag37t-nwS6NlS3r139xBRC4X2wuKtg130_assertion type Assertion NP378015.RAFNqFHHI6QrNUoag37t-nwS6NlS3r139xBRC4X2wuKtg130_head.
- 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.