Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP610359.RAwh6nSeGobWgZE92D7qTq59aYZce8nAwvCRmgv6QkauY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP610359.RAwh6nSeGobWgZE92D7qTq59aYZce8nAwvCRmgv6QkauY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP610359.RAwh6nSeGobWgZE92D7qTq59aYZce8nAwvCRmgv6QkauY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP610359.RAwh6nSeGobWgZE92D7qTq59aYZce8nAwvCRmgv6QkauY130_provenance.
- NP610359.RAwh6nSeGobWgZE92D7qTq59aYZce8nAwvCRmgv6QkauY130_assertion description "[Mutations in PAX6 gene have been shown to be the genetic cause of aniridia, which is a severe panocular eye disease characterised by iris hypoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP610359.RAwh6nSeGobWgZE92D7qTq59aYZce8nAwvCRmgv6QkauY130_provenance.
- NP610359.RAwh6nSeGobWgZE92D7qTq59aYZce8nAwvCRmgv6QkauY130_assertion evidence source_evidence_literature NP610359.RAwh6nSeGobWgZE92D7qTq59aYZce8nAwvCRmgv6QkauY130_provenance.
- NP610359.RAwh6nSeGobWgZE92D7qTq59aYZce8nAwvCRmgv6QkauY130_assertion SIO_000772 15740668 NP610359.RAwh6nSeGobWgZE92D7qTq59aYZce8nAwvCRmgv6QkauY130_provenance.
- NP610359.RAwh6nSeGobWgZE92D7qTq59aYZce8nAwvCRmgv6QkauY130_assertion wasDerivedFrom befree-20150227 NP610359.RAwh6nSeGobWgZE92D7qTq59aYZce8nAwvCRmgv6QkauY130_provenance.
- NP610359.RAwh6nSeGobWgZE92D7qTq59aYZce8nAwvCRmgv6QkauY130_assertion wasGeneratedBy ECO_0000203 NP610359.RAwh6nSeGobWgZE92D7qTq59aYZce8nAwvCRmgv6QkauY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP610359.RAwh6nSeGobWgZE92D7qTq59aYZce8nAwvCRmgv6QkauY130_provenance.