Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP614861.RA3gbk5M631N7jMw2vq2-Z9rZHT8WoDJq7wnikqVetvOg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP614861.RA3gbk5M631N7jMw2vq2-Z9rZHT8WoDJq7wnikqVetvOg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP614861.RA3gbk5M631N7jMw2vq2-Z9rZHT8WoDJq7wnikqVetvOg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP614861.RA3gbk5M631N7jMw2vq2-Z9rZHT8WoDJq7wnikqVetvOg130_provenance.
- befree-2016 importedOn "2016-02-19" NP614861.RA3gbk5M631N7jMw2vq2-Z9rZHT8WoDJq7wnikqVetvOg130_provenance.
- 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.