Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP452294.RAYdqYOlWbGwCzEKzH2C0dKE1n45xF0R86wA0zjUzw60k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP452294.RAYdqYOlWbGwCzEKzH2C0dKE1n45xF0R86wA0zjUzw60k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP452294.RAYdqYOlWbGwCzEKzH2C0dKE1n45xF0R86wA0zjUzw60k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP452294.RAYdqYOlWbGwCzEKzH2C0dKE1n45xF0R86wA0zjUzw60k130_provenance.
- befree-2016 importedOn "2016-02-19" NP452294.RAYdqYOlWbGwCzEKzH2C0dKE1n45xF0R86wA0zjUzw60k130_provenance.
- NP452294.RAYdqYOlWbGwCzEKzH2C0dKE1n45xF0R86wA0zjUzw60k130_assertion wasGeneratedBy ECO_0000203 NP452294.RAYdqYOlWbGwCzEKzH2C0dKE1n45xF0R86wA0zjUzw60k130_provenance.
- NP452294.RAYdqYOlWbGwCzEKzH2C0dKE1n45xF0R86wA0zjUzw60k130_assertion wasDerivedFrom befree-2016 NP452294.RAYdqYOlWbGwCzEKzH2C0dKE1n45xF0R86wA0zjUzw60k130_provenance.
- NP452294.RAYdqYOlWbGwCzEKzH2C0dKE1n45xF0R86wA0zjUzw60k130_assertion SIO_000772 15257456 NP452294.RAYdqYOlWbGwCzEKzH2C0dKE1n45xF0R86wA0zjUzw60k130_provenance.
- NP452294.RAYdqYOlWbGwCzEKzH2C0dKE1n45xF0R86wA0zjUzw60k130_assertion evidence source_evidence_literature NP452294.RAYdqYOlWbGwCzEKzH2C0dKE1n45xF0R86wA0zjUzw60k130_provenance.
- NP452294.RAYdqYOlWbGwCzEKzH2C0dKE1n45xF0R86wA0zjUzw60k130_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." NP452294.RAYdqYOlWbGwCzEKzH2C0dKE1n45xF0R86wA0zjUzw60k130_provenance.