Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP584146.RA1gkbbX2xxaWjAB38O8wTQJ3hp1CigTslKOWKgJ5ndaE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP584146.RA1gkbbX2xxaWjAB38O8wTQJ3hp1CigTslKOWKgJ5ndaE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP584146.RA1gkbbX2xxaWjAB38O8wTQJ3hp1CigTslKOWKgJ5ndaE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP584146.RA1gkbbX2xxaWjAB38O8wTQJ3hp1CigTslKOWKgJ5ndaE130_provenance.
- NP584146.RA1gkbbX2xxaWjAB38O8wTQJ3hp1CigTslKOWKgJ5ndaE130_assertion description "[To evaluate visual impairment in Finnish Usher syndrome type 3 (USH3) and compare this with visual impairment in Usher syndrome types 1b (USH1b) and 2a (USH2a).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584146.RA1gkbbX2xxaWjAB38O8wTQJ3hp1CigTslKOWKgJ5ndaE130_provenance.
- NP584146.RA1gkbbX2xxaWjAB38O8wTQJ3hp1CigTslKOWKgJ5ndaE130_assertion evidence source_evidence_literature NP584146.RA1gkbbX2xxaWjAB38O8wTQJ3hp1CigTslKOWKgJ5ndaE130_provenance.
- NP584146.RA1gkbbX2xxaWjAB38O8wTQJ3hp1CigTslKOWKgJ5ndaE130_assertion SIO_000772 16445437 NP584146.RA1gkbbX2xxaWjAB38O8wTQJ3hp1CigTslKOWKgJ5ndaE130_provenance.
- NP584146.RA1gkbbX2xxaWjAB38O8wTQJ3hp1CigTslKOWKgJ5ndaE130_assertion wasDerivedFrom befree-20150227 NP584146.RA1gkbbX2xxaWjAB38O8wTQJ3hp1CigTslKOWKgJ5ndaE130_provenance.
- NP584146.RA1gkbbX2xxaWjAB38O8wTQJ3hp1CigTslKOWKgJ5ndaE130_assertion wasGeneratedBy ECO_0000203 NP584146.RA1gkbbX2xxaWjAB38O8wTQJ3hp1CigTslKOWKgJ5ndaE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP584146.RA1gkbbX2xxaWjAB38O8wTQJ3hp1CigTslKOWKgJ5ndaE130_provenance.