Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP985396.RADEt5VNGnv9YRNz1ggp4j0N0stiFYg5qS8zAaTjv5t4s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP985396.RADEt5VNGnv9YRNz1ggp4j0N0stiFYg5qS8zAaTjv5t4s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP985396.RADEt5VNGnv9YRNz1ggp4j0N0stiFYg5qS8zAaTjv5t4s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP985396.RADEt5VNGnv9YRNz1ggp4j0N0stiFYg5qS8zAaTjv5t4s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP985396.RADEt5VNGnv9YRNz1ggp4j0N0stiFYg5qS8zAaTjv5t4s130_provenance.
- 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.