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- NP581768.RAr1JwVANJYXKYH9l7Gm2zqqYNRbTKijNTEmwDPvQkFIk130_assertion type Assertion NP581768.RAr1JwVANJYXKYH9l7Gm2zqqYNRbTKijNTEmwDPvQkFIk130_head.
- NP581768.RAr1JwVANJYXKYH9l7Gm2zqqYNRbTKijNTEmwDPvQkFIk130_assertion wasGeneratedBy ECO_0000203 NP581768.RAr1JwVANJYXKYH9l7Gm2zqqYNRbTKijNTEmwDPvQkFIk130_provenance.
- NP581768.RAr1JwVANJYXKYH9l7Gm2zqqYNRbTKijNTEmwDPvQkFIk130_assertion wasDerivedFrom befree-20140225 NP581768.RAr1JwVANJYXKYH9l7Gm2zqqYNRbTKijNTEmwDPvQkFIk130_provenance.
- NP581768.RAr1JwVANJYXKYH9l7Gm2zqqYNRbTKijNTEmwDPvQkFIk130_assertion SIO_000772 17431911 NP581768.RAr1JwVANJYXKYH9l7Gm2zqqYNRbTKijNTEmwDPvQkFIk130_provenance.
- NP581768.RAr1JwVANJYXKYH9l7Gm2zqqYNRbTKijNTEmwDPvQkFIk130_assertion evidence source_evidence_literature NP581768.RAr1JwVANJYXKYH9l7Gm2zqqYNRbTKijNTEmwDPvQkFIk130_provenance.
- NP581768.RAr1JwVANJYXKYH9l7Gm2zqqYNRbTKijNTEmwDPvQkFIk130_assertion description "[Contiguous deletion of the NDP, MAOA, MAOB, and EFHC2 genes in a patient with Norrie disease, severe psychomotor retardation and myoclonic epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP581768.RAr1JwVANJYXKYH9l7Gm2zqqYNRbTKijNTEmwDPvQkFIk130_provenance.