Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP614861.RA3gbk5M631N7jMw2vq2-Z9rZHT8WoDJq7wnikqVetvOg130_assertion> ?p ?o ?g. }
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- NP614861.RA3gbk5M631N7jMw2vq2-Z9rZHT8WoDJq7wnikqVetvOg130_assertion type Assertion NP614861.RA3gbk5M631N7jMw2vq2-Z9rZHT8WoDJq7wnikqVetvOg130_head.
- NP614861.RA3gbk5M631N7jMw2vq2-Z9rZHT8WoDJq7wnikqVetvOg130_assertion wasGeneratedBy ECO_0000203 NP614861.RA3gbk5M631N7jMw2vq2-Z9rZHT8WoDJq7wnikqVetvOg130_provenance.
- NP614861.RA3gbk5M631N7jMw2vq2-Z9rZHT8WoDJq7wnikqVetvOg130_assertion wasDerivedFrom befree-2016 NP614861.RA3gbk5M631N7jMw2vq2-Z9rZHT8WoDJq7wnikqVetvOg130_provenance.
- NP614861.RA3gbk5M631N7jMw2vq2-Z9rZHT8WoDJq7wnikqVetvOg130_assertion SIO_000772 17564961 NP614861.RA3gbk5M631N7jMw2vq2-Z9rZHT8WoDJq7wnikqVetvOg130_provenance.
- NP614861.RA3gbk5M631N7jMw2vq2-Z9rZHT8WoDJq7wnikqVetvOg130_assertion evidence source_evidence_literature NP614861.RA3gbk5M631N7jMw2vq2-Z9rZHT8WoDJq7wnikqVetvOg130_provenance.
- NP614861.RA3gbk5M631N7jMw2vq2-Z9rZHT8WoDJq7wnikqVetvOg130_assertion description "[We identified a mutation in the CRYGD gene (P23S) of the gamma-crystallin gene cluster that is associated with a polymorphic congenital cataract that occurs with frequency of approximately 0.3% in a human population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP614861.RA3gbk5M631N7jMw2vq2-Z9rZHT8WoDJq7wnikqVetvOg130_provenance.