Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP818990.RAO5JP6wlhP0yAVI1WqiomJ5Js3PVL2T7akddv0Fe5lYY130_assertion> ?p ?o ?g. }
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- NP818990.RAO5JP6wlhP0yAVI1WqiomJ5Js3PVL2T7akddv0Fe5lYY130_assertion type Assertion NP818990.RAO5JP6wlhP0yAVI1WqiomJ5Js3PVL2T7akddv0Fe5lYY130_head.
- NP818990.RAO5JP6wlhP0yAVI1WqiomJ5Js3PVL2T7akddv0Fe5lYY130_assertion description "[This study reveals that mutations in the ADAMTS18 gene can cause a broad phenotypic spectrum of eye disorders and contribute to shed further light on the complexity of retinal diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP818990.RAO5JP6wlhP0yAVI1WqiomJ5Js3PVL2T7akddv0Fe5lYY130_provenance.
- NP818990.RAO5JP6wlhP0yAVI1WqiomJ5Js3PVL2T7akddv0Fe5lYY130_assertion evidence source_evidence_literature NP818990.RAO5JP6wlhP0yAVI1WqiomJ5Js3PVL2T7akddv0Fe5lYY130_provenance.
- NP818990.RAO5JP6wlhP0yAVI1WqiomJ5Js3PVL2T7akddv0Fe5lYY130_assertion SIO_000772 23356391 NP818990.RAO5JP6wlhP0yAVI1WqiomJ5Js3PVL2T7akddv0Fe5lYY130_provenance.
- NP818990.RAO5JP6wlhP0yAVI1WqiomJ5Js3PVL2T7akddv0Fe5lYY130_assertion wasDerivedFrom befree-20140225 NP818990.RAO5JP6wlhP0yAVI1WqiomJ5Js3PVL2T7akddv0Fe5lYY130_provenance.
- NP818990.RAO5JP6wlhP0yAVI1WqiomJ5Js3PVL2T7akddv0Fe5lYY130_assertion wasGeneratedBy ECO_0000203 NP818990.RAO5JP6wlhP0yAVI1WqiomJ5Js3PVL2T7akddv0Fe5lYY130_provenance.