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- NP29517.RAU1zZ1n8tABz0aEpuX0L_moU1itNf4EG6aXkqIxo3eJY130_assertion type Assertion NP29517.RAU1zZ1n8tABz0aEpuX0L_moU1itNf4EG6aXkqIxo3eJY130_head.
- NP29517.RAU1zZ1n8tABz0aEpuX0L_moU1itNf4EG6aXkqIxo3eJY130_assertion description "[De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29517.RAU1zZ1n8tABz0aEpuX0L_moU1itNf4EG6aXkqIxo3eJY130_provenance.
- NP29517.RAU1zZ1n8tABz0aEpuX0L_moU1itNf4EG6aXkqIxo3eJY130_assertion evidence source_evidence_curated NP29517.RAU1zZ1n8tABz0aEpuX0L_moU1itNf4EG6aXkqIxo3eJY130_provenance.
- NP29517.RAU1zZ1n8tABz0aEpuX0L_moU1itNf4EG6aXkqIxo3eJY130_assertion SIO_000772 21706002 NP29517.RAU1zZ1n8tABz0aEpuX0L_moU1itNf4EG6aXkqIxo3eJY130_provenance.
- NP29517.RAU1zZ1n8tABz0aEpuX0L_moU1itNf4EG6aXkqIxo3eJY130_assertion wasDerivedFrom ctd_human-2016 NP29517.RAU1zZ1n8tABz0aEpuX0L_moU1itNf4EG6aXkqIxo3eJY130_provenance.
- NP29517.RAU1zZ1n8tABz0aEpuX0L_moU1itNf4EG6aXkqIxo3eJY130_assertion wasGeneratedBy ECO_0000218 NP29517.RAU1zZ1n8tABz0aEpuX0L_moU1itNf4EG6aXkqIxo3eJY130_provenance.