Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP534198.RAwmhpxKR-1olJc7IjAZ61DBNWVl4TvwttHt1Y65rSEHU130_assertion> ?p ?o ?g. }
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- NP534198.RAwmhpxKR-1olJc7IjAZ61DBNWVl4TvwttHt1Y65rSEHU130_assertion type Assertion NP534198.RAwmhpxKR-1olJc7IjAZ61DBNWVl4TvwttHt1Y65rSEHU130_head.
- NP534198.RAwmhpxKR-1olJc7IjAZ61DBNWVl4TvwttHt1Y65rSEHU130_assertion description "[Congenital cataract and macular hypoplasia in humans associated with a de novo mutation in CRYAA and compound heterozygous mutations in P.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP534198.RAwmhpxKR-1olJc7IjAZ61DBNWVl4TvwttHt1Y65rSEHU130_provenance.
- NP534198.RAwmhpxKR-1olJc7IjAZ61DBNWVl4TvwttHt1Y65rSEHU130_assertion evidence source_evidence_literature NP534198.RAwmhpxKR-1olJc7IjAZ61DBNWVl4TvwttHt1Y65rSEHU130_provenance.
- NP534198.RAwmhpxKR-1olJc7IjAZ61DBNWVl4TvwttHt1Y65rSEHU130_assertion SIO_000772 16453125 NP534198.RAwmhpxKR-1olJc7IjAZ61DBNWVl4TvwttHt1Y65rSEHU130_provenance.
- NP534198.RAwmhpxKR-1olJc7IjAZ61DBNWVl4TvwttHt1Y65rSEHU130_assertion wasDerivedFrom befree-2016 NP534198.RAwmhpxKR-1olJc7IjAZ61DBNWVl4TvwttHt1Y65rSEHU130_provenance.
- NP534198.RAwmhpxKR-1olJc7IjAZ61DBNWVl4TvwttHt1Y65rSEHU130_assertion wasGeneratedBy ECO_0000203 NP534198.RAwmhpxKR-1olJc7IjAZ61DBNWVl4TvwttHt1Y65rSEHU130_provenance.