Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP985396.RADEt5VNGnv9YRNz1ggp4j0N0stiFYg5qS8zAaTjv5t4s130_assertion> ?p ?o ?g. }
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- NP985396.RADEt5VNGnv9YRNz1ggp4j0N0stiFYg5qS8zAaTjv5t4s130_assertion type Assertion NP985396.RADEt5VNGnv9YRNz1ggp4j0N0stiFYg5qS8zAaTjv5t4s130_head.
- NP985396.RADEt5VNGnv9YRNz1ggp4j0N0stiFYg5qS8zAaTjv5t4s130_assertion wasGeneratedBy ECO_0000203 NP985396.RADEt5VNGnv9YRNz1ggp4j0N0stiFYg5qS8zAaTjv5t4s130_provenance.
- NP985396.RADEt5VNGnv9YRNz1ggp4j0N0stiFYg5qS8zAaTjv5t4s130_assertion wasDerivedFrom befree-20150227 NP985396.RADEt5VNGnv9YRNz1ggp4j0N0stiFYg5qS8zAaTjv5t4s130_provenance.
- NP985396.RADEt5VNGnv9YRNz1ggp4j0N0stiFYg5qS8zAaTjv5t4s130_assertion SIO_000772 15257456 NP985396.RADEt5VNGnv9YRNz1ggp4j0N0stiFYg5qS8zAaTjv5t4s130_provenance.
- NP985396.RADEt5VNGnv9YRNz1ggp4j0N0stiFYg5qS8zAaTjv5t4s130_assertion evidence source_evidence_literature NP985396.RADEt5VNGnv9YRNz1ggp4j0N0stiFYg5qS8zAaTjv5t4s130_provenance.
- NP985396.RADEt5VNGnv9YRNz1ggp4j0N0stiFYg5qS8zAaTjv5t4s130_assertion description "[It has been previously shown that mutations in a particular nucleotide in CHX10 are associated with an autosomal recessive syndrome of microphthalmia/anophthalmia with iris colobomas and cataracts in two families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP985396.RADEt5VNGnv9YRNz1ggp4j0N0stiFYg5qS8zAaTjv5t4s130_provenance.