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- NP426442.RAYwWEcC5jDdht0kiWvFwpf4S12FE1nQYe94ct9QYRJKg130_assertion type Assertion NP426442.RAYwWEcC5jDdht0kiWvFwpf4S12FE1nQYe94ct9QYRJKg130_head.
- NP426442.RAYwWEcC5jDdht0kiWvFwpf4S12FE1nQYe94ct9QYRJKg130_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." NP426442.RAYwWEcC5jDdht0kiWvFwpf4S12FE1nQYe94ct9QYRJKg130_provenance.
- NP426442.RAYwWEcC5jDdht0kiWvFwpf4S12FE1nQYe94ct9QYRJKg130_assertion evidence source_evidence_literature NP426442.RAYwWEcC5jDdht0kiWvFwpf4S12FE1nQYe94ct9QYRJKg130_provenance.
- NP426442.RAYwWEcC5jDdht0kiWvFwpf4S12FE1nQYe94ct9QYRJKg130_assertion SIO_000772 11174420 NP426442.RAYwWEcC5jDdht0kiWvFwpf4S12FE1nQYe94ct9QYRJKg130_provenance.
- NP426442.RAYwWEcC5jDdht0kiWvFwpf4S12FE1nQYe94ct9QYRJKg130_assertion wasDerivedFrom befree-20150227 NP426442.RAYwWEcC5jDdht0kiWvFwpf4S12FE1nQYe94ct9QYRJKg130_provenance.
- NP426442.RAYwWEcC5jDdht0kiWvFwpf4S12FE1nQYe94ct9QYRJKg130_assertion wasGeneratedBy ECO_0000203 NP426442.RAYwWEcC5jDdht0kiWvFwpf4S12FE1nQYe94ct9QYRJKg130_provenance.