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- NP609790.RAswaJ-sM6unjCV4rBbKuOiXb77gKtbQ4CML8IQ-sGvn4130_assertion type Assertion NP609790.RAswaJ-sM6unjCV4rBbKuOiXb77gKtbQ4CML8IQ-sGvn4130_head.
- NP609790.RAswaJ-sM6unjCV4rBbKuOiXb77gKtbQ4CML8IQ-sGvn4130_assertion wasGeneratedBy ECO_0000203 NP609790.RAswaJ-sM6unjCV4rBbKuOiXb77gKtbQ4CML8IQ-sGvn4130_provenance.
- NP609790.RAswaJ-sM6unjCV4rBbKuOiXb77gKtbQ4CML8IQ-sGvn4130_assertion wasDerivedFrom befree-20140225 NP609790.RAswaJ-sM6unjCV4rBbKuOiXb77gKtbQ4CML8IQ-sGvn4130_provenance.
- NP609790.RAswaJ-sM6unjCV4rBbKuOiXb77gKtbQ4CML8IQ-sGvn4130_assertion SIO_000772 8075643 NP609790.RAswaJ-sM6unjCV4rBbKuOiXb77gKtbQ4CML8IQ-sGvn4130_provenance.
- NP609790.RAswaJ-sM6unjCV4rBbKuOiXb77gKtbQ4CML8IQ-sGvn4130_assertion evidence source_evidence_literature NP609790.RAswaJ-sM6unjCV4rBbKuOiXb77gKtbQ4CML8IQ-sGvn4130_provenance.
- NP609790.RAswaJ-sM6unjCV4rBbKuOiXb77gKtbQ4CML8IQ-sGvn4130_assertion description "[Homozygous nonsense mutations in the beta PDE gene have been found recently in patients with autosomal recessive retinitis pigmentosa, a common hereditary photoreceptor dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP609790.RAswaJ-sM6unjCV4rBbKuOiXb77gKtbQ4CML8IQ-sGvn4130_provenance.