Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP771961.RACytf7JJ0qLAFSAzfKSjyTLwiQbD72xmLC4rwaBdyI0Q130_assertion> ?p ?o ?g. }
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- NP771961.RACytf7JJ0qLAFSAzfKSjyTLwiQbD72xmLC4rwaBdyI0Q130_assertion type Assertion NP771961.RACytf7JJ0qLAFSAzfKSjyTLwiQbD72xmLC4rwaBdyI0Q130_head.
- NP771961.RACytf7JJ0qLAFSAzfKSjyTLwiQbD72xmLC4rwaBdyI0Q130_assertion wasGeneratedBy ECO_0000203 NP771961.RACytf7JJ0qLAFSAzfKSjyTLwiQbD72xmLC4rwaBdyI0Q130_provenance.
- NP771961.RACytf7JJ0qLAFSAzfKSjyTLwiQbD72xmLC4rwaBdyI0Q130_assertion wasDerivedFrom befree-2016 NP771961.RACytf7JJ0qLAFSAzfKSjyTLwiQbD72xmLC4rwaBdyI0Q130_provenance.
- NP771961.RACytf7JJ0qLAFSAzfKSjyTLwiQbD72xmLC4rwaBdyI0Q130_assertion SIO_000772 19860667 NP771961.RACytf7JJ0qLAFSAzfKSjyTLwiQbD72xmLC4rwaBdyI0Q130_provenance.
- NP771961.RACytf7JJ0qLAFSAzfKSjyTLwiQbD72xmLC4rwaBdyI0Q130_assertion evidence source_evidence_literature NP771961.RACytf7JJ0qLAFSAzfKSjyTLwiQbD72xmLC4rwaBdyI0Q130_provenance.
- NP771961.RACytf7JJ0qLAFSAzfKSjyTLwiQbD72xmLC4rwaBdyI0Q130_assertion description "[Non-syndromic, hereditary human cataract development is linked to point mutations in the CRYAA and CRYAB genes which encode alphaA and alphaB-crystallin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP771961.RACytf7JJ0qLAFSAzfKSjyTLwiQbD72xmLC4rwaBdyI0Q130_provenance.