Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP641541.RA0uuhXn6xVJtpl4dbJweWlFB912MTSRoWl6_vS6s8AGg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP641541.RA0uuhXn6xVJtpl4dbJweWlFB912MTSRoWl6_vS6s8AGg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP641541.RA0uuhXn6xVJtpl4dbJweWlFB912MTSRoWl6_vS6s8AGg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP641541.RA0uuhXn6xVJtpl4dbJweWlFB912MTSRoWl6_vS6s8AGg130_provenance.
- NP641541.RA0uuhXn6xVJtpl4dbJweWlFB912MTSRoWl6_vS6s8AGg130_assertion wasGeneratedBy ECO_0000203 NP641541.RA0uuhXn6xVJtpl4dbJweWlFB912MTSRoWl6_vS6s8AGg130_provenance.
- NP641541.RA0uuhXn6xVJtpl4dbJweWlFB912MTSRoWl6_vS6s8AGg130_assertion wasDerivedFrom befree-20140225 NP641541.RA0uuhXn6xVJtpl4dbJweWlFB912MTSRoWl6_vS6s8AGg130_provenance.
- NP641541.RA0uuhXn6xVJtpl4dbJweWlFB912MTSRoWl6_vS6s8AGg130_assertion SIO_000772 9662395 NP641541.RA0uuhXn6xVJtpl4dbJweWlFB912MTSRoWl6_vS6s8AGg130_provenance.
- NP641541.RA0uuhXn6xVJtpl4dbJweWlFB912MTSRoWl6_vS6s8AGg130_assertion evidence source_evidence_literature NP641541.RA0uuhXn6xVJtpl4dbJweWlFB912MTSRoWl6_vS6s8AGg130_provenance.
- NP641541.RA0uuhXn6xVJtpl4dbJweWlFB912MTSRoWl6_vS6s8AGg130_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." NP641541.RA0uuhXn6xVJtpl4dbJweWlFB912MTSRoWl6_vS6s8AGg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP641541.RA0uuhXn6xVJtpl4dbJweWlFB912MTSRoWl6_vS6s8AGg130_provenance.