Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP775467.RAA2BUmy0NnRp2-0Q8abodCi-W-XYPkR0yV9syo1tdOtk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP775467.RAA2BUmy0NnRp2-0Q8abodCi-W-XYPkR0yV9syo1tdOtk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP775467.RAA2BUmy0NnRp2-0Q8abodCi-W-XYPkR0yV9syo1tdOtk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP775467.RAA2BUmy0NnRp2-0Q8abodCi-W-XYPkR0yV9syo1tdOtk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP775467.RAA2BUmy0NnRp2-0Q8abodCi-W-XYPkR0yV9syo1tdOtk130_provenance.
- NP775467.RAA2BUmy0NnRp2-0Q8abodCi-W-XYPkR0yV9syo1tdOtk130_assertion wasGeneratedBy ECO_0000203 NP775467.RAA2BUmy0NnRp2-0Q8abodCi-W-XYPkR0yV9syo1tdOtk130_provenance.
- NP775467.RAA2BUmy0NnRp2-0Q8abodCi-W-XYPkR0yV9syo1tdOtk130_assertion wasDerivedFrom befree-20150227 NP775467.RAA2BUmy0NnRp2-0Q8abodCi-W-XYPkR0yV9syo1tdOtk130_provenance.
- NP775467.RAA2BUmy0NnRp2-0Q8abodCi-W-XYPkR0yV9syo1tdOtk130_assertion SIO_000772 24560797 NP775467.RAA2BUmy0NnRp2-0Q8abodCi-W-XYPkR0yV9syo1tdOtk130_provenance.
- NP775467.RAA2BUmy0NnRp2-0Q8abodCi-W-XYPkR0yV9syo1tdOtk130_assertion evidence source_evidence_literature NP775467.RAA2BUmy0NnRp2-0Q8abodCi-W-XYPkR0yV9syo1tdOtk130_provenance.
- NP775467.RAA2BUmy0NnRp2-0Q8abodCi-W-XYPkR0yV9syo1tdOtk130_assertion description "[Mutations in BEST1 cause five distinct retinal degenerative diseases, including adult vitelliform macular dystrophy (AVMD), autosomal recessive bestrophinopathy (ARB), autosomal dominant vitreoretinochoroidopathy (ADVIRC), and retinitis pigmentosa (RP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP775467.RAA2BUmy0NnRp2-0Q8abodCi-W-XYPkR0yV9syo1tdOtk130_provenance.