Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1018535.RADG6zkDLE24zsWOEki3kVuP5oioVD8zIjqrSDWqWYpp8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1018535.RADG6zkDLE24zsWOEki3kVuP5oioVD8zIjqrSDWqWYpp8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1018535.RADG6zkDLE24zsWOEki3kVuP5oioVD8zIjqrSDWqWYpp8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1018535.RADG6zkDLE24zsWOEki3kVuP5oioVD8zIjqrSDWqWYpp8130_provenance.
- NP1018535.RADG6zkDLE24zsWOEki3kVuP5oioVD8zIjqrSDWqWYpp8130_assertion description "[Congenital cataract and macular hypoplasia in humans associated with a de novo mutation in CRYAA and compound heterozygous mutations in P.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1018535.RADG6zkDLE24zsWOEki3kVuP5oioVD8zIjqrSDWqWYpp8130_provenance.
- NP1018535.RADG6zkDLE24zsWOEki3kVuP5oioVD8zIjqrSDWqWYpp8130_assertion evidence source_evidence_literature NP1018535.RADG6zkDLE24zsWOEki3kVuP5oioVD8zIjqrSDWqWYpp8130_provenance.
- NP1018535.RADG6zkDLE24zsWOEki3kVuP5oioVD8zIjqrSDWqWYpp8130_assertion SIO_000772 16453125 NP1018535.RADG6zkDLE24zsWOEki3kVuP5oioVD8zIjqrSDWqWYpp8130_provenance.
- NP1018535.RADG6zkDLE24zsWOEki3kVuP5oioVD8zIjqrSDWqWYpp8130_assertion wasDerivedFrom befree-20150227 NP1018535.RADG6zkDLE24zsWOEki3kVuP5oioVD8zIjqrSDWqWYpp8130_provenance.
- NP1018535.RADG6zkDLE24zsWOEki3kVuP5oioVD8zIjqrSDWqWYpp8130_assertion wasGeneratedBy ECO_0000203 NP1018535.RADG6zkDLE24zsWOEki3kVuP5oioVD8zIjqrSDWqWYpp8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1018535.RADG6zkDLE24zsWOEki3kVuP5oioVD8zIjqrSDWqWYpp8130_provenance.