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- NP1143489.RAqFfEZYiYQATr1Lm5cItwV_19Z1ycyg7e7wbgWZpMHhs130_assertion type Assertion NP1143489.RAqFfEZYiYQATr1Lm5cItwV_19Z1ycyg7e7wbgWZpMHhs130_head.
- NP1143489.RAqFfEZYiYQATr1Lm5cItwV_19Z1ycyg7e7wbgWZpMHhs130_assertion wasGeneratedBy ECO_0000203 NP1143489.RAqFfEZYiYQATr1Lm5cItwV_19Z1ycyg7e7wbgWZpMHhs130_provenance.
- NP1143489.RAqFfEZYiYQATr1Lm5cItwV_19Z1ycyg7e7wbgWZpMHhs130_assertion wasDerivedFrom befree-2016 NP1143489.RAqFfEZYiYQATr1Lm5cItwV_19Z1ycyg7e7wbgWZpMHhs130_provenance.
- NP1143489.RAqFfEZYiYQATr1Lm5cItwV_19Z1ycyg7e7wbgWZpMHhs130_assertion SIO_000772 24405844 NP1143489.RAqFfEZYiYQATr1Lm5cItwV_19Z1ycyg7e7wbgWZpMHhs130_provenance.
- NP1143489.RAqFfEZYiYQATr1Lm5cItwV_19Z1ycyg7e7wbgWZpMHhs130_assertion evidence source_evidence_literature NP1143489.RAqFfEZYiYQATr1Lm5cItwV_19Z1ycyg7e7wbgWZpMHhs130_provenance.
- NP1143489.RAqFfEZYiYQATr1Lm5cItwV_19Z1ycyg7e7wbgWZpMHhs130_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." NP1143489.RAqFfEZYiYQATr1Lm5cItwV_19Z1ycyg7e7wbgWZpMHhs130_provenance.