Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1399284.RAAqqSW2-Mc0wlZDSrddBXpyX3TMv7jfJ_4sFSTPYY1tw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1399284.RAAqqSW2-Mc0wlZDSrddBXpyX3TMv7jfJ_4sFSTPYY1tw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1399284.RAAqqSW2-Mc0wlZDSrddBXpyX3TMv7jfJ_4sFSTPYY1tw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1399284.RAAqqSW2-Mc0wlZDSrddBXpyX3TMv7jfJ_4sFSTPYY1tw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1399284.RAAqqSW2-Mc0wlZDSrddBXpyX3TMv7jfJ_4sFSTPYY1tw130_provenance.
- NP1399284.RAAqqSW2-Mc0wlZDSrddBXpyX3TMv7jfJ_4sFSTPYY1tw130_assertion wasGeneratedBy ECO_0000203 NP1399284.RAAqqSW2-Mc0wlZDSrddBXpyX3TMv7jfJ_4sFSTPYY1tw130_provenance.
- NP1399284.RAAqqSW2-Mc0wlZDSrddBXpyX3TMv7jfJ_4sFSTPYY1tw130_assertion wasDerivedFrom befree-2016 NP1399284.RAAqqSW2-Mc0wlZDSrddBXpyX3TMv7jfJ_4sFSTPYY1tw130_provenance.
- NP1399284.RAAqqSW2-Mc0wlZDSrddBXpyX3TMv7jfJ_4sFSTPYY1tw130_assertion SIO_000772 9662395 NP1399284.RAAqqSW2-Mc0wlZDSrddBXpyX3TMv7jfJ_4sFSTPYY1tw130_provenance.
- NP1399284.RAAqqSW2-Mc0wlZDSrddBXpyX3TMv7jfJ_4sFSTPYY1tw130_assertion evidence source_evidence_literature NP1399284.RAAqqSW2-Mc0wlZDSrddBXpyX3TMv7jfJ_4sFSTPYY1tw130_provenance.
- NP1399284.RAAqqSW2-Mc0wlZDSrddBXpyX3TMv7jfJ_4sFSTPYY1tw130_assertion description "[Best macular dystrophy (BMD), also known as vitelliform macular dystrophy (VMD2; OMIM 153700), is an autosomal dominant form of macular degeneration characterized by an abnormal accumulation of lipofuscin within and beneath the retinal pigment epithelium cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1399284.RAAqqSW2-Mc0wlZDSrddBXpyX3TMv7jfJ_4sFSTPYY1tw130_provenance.