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- NP557016.RAT-vqC9JoeRbFPQJQYOrj7tZ4gODv0Y5SttIa-ZfBT7I130_assertion type Assertion NP557016.RAT-vqC9JoeRbFPQJQYOrj7tZ4gODv0Y5SttIa-ZfBT7I130_head.
- NP557016.RAT-vqC9JoeRbFPQJQYOrj7tZ4gODv0Y5SttIa-ZfBT7I130_assertion wasGeneratedBy ECO_0000203 NP557016.RAT-vqC9JoeRbFPQJQYOrj7tZ4gODv0Y5SttIa-ZfBT7I130_provenance.
- NP557016.RAT-vqC9JoeRbFPQJQYOrj7tZ4gODv0Y5SttIa-ZfBT7I130_assertion wasDerivedFrom befree-20150227 NP557016.RAT-vqC9JoeRbFPQJQYOrj7tZ4gODv0Y5SttIa-ZfBT7I130_provenance.
- NP557016.RAT-vqC9JoeRbFPQJQYOrj7tZ4gODv0Y5SttIa-ZfBT7I130_assertion SIO_000772 24405844 NP557016.RAT-vqC9JoeRbFPQJQYOrj7tZ4gODv0Y5SttIa-ZfBT7I130_provenance.
- NP557016.RAT-vqC9JoeRbFPQJQYOrj7tZ4gODv0Y5SttIa-ZfBT7I130_assertion evidence source_evidence_literature NP557016.RAT-vqC9JoeRbFPQJQYOrj7tZ4gODv0Y5SttIa-ZfBT7I130_provenance.
- NP557016.RAT-vqC9JoeRbFPQJQYOrj7tZ4gODv0Y5SttIa-ZfBT7I130_assertion description "[A novel MIP gene mutation associated with autosomal dominant congenital cataracts in a Chinese family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557016.RAT-vqC9JoeRbFPQJQYOrj7tZ4gODv0Y5SttIa-ZfBT7I130_provenance.