Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP353267.RANJc_UIp-_65-Kp4JIrGfR4OFzSsKNRY2cqVMYOTtcnU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP353267.RANJc_UIp-_65-Kp4JIrGfR4OFzSsKNRY2cqVMYOTtcnU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP353267.RANJc_UIp-_65-Kp4JIrGfR4OFzSsKNRY2cqVMYOTtcnU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP353267.RANJc_UIp-_65-Kp4JIrGfR4OFzSsKNRY2cqVMYOTtcnU130_provenance.
- NP353267.RANJc_UIp-_65-Kp4JIrGfR4OFzSsKNRY2cqVMYOTtcnU130_assertion description "[Vitelliform macular dystrophy (VMD2, Best disease, MIM153700) is an early onset, autosomal, dominant macular degeneration characterized by the deposition of lipofuscin-like material within and below the retinal pigment epithelium (RPE); it is associated with degeneration of the RPE and overlying photoreceptors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP353267.RANJc_UIp-_65-Kp4JIrGfR4OFzSsKNRY2cqVMYOTtcnU130_provenance.
- NP353267.RANJc_UIp-_65-Kp4JIrGfR4OFzSsKNRY2cqVMYOTtcnU130_assertion evidence source_evidence_literature NP353267.RANJc_UIp-_65-Kp4JIrGfR4OFzSsKNRY2cqVMYOTtcnU130_provenance.
- NP353267.RANJc_UIp-_65-Kp4JIrGfR4OFzSsKNRY2cqVMYOTtcnU130_assertion SIO_000772 10453731 NP353267.RANJc_UIp-_65-Kp4JIrGfR4OFzSsKNRY2cqVMYOTtcnU130_provenance.
- NP353267.RANJc_UIp-_65-Kp4JIrGfR4OFzSsKNRY2cqVMYOTtcnU130_assertion wasDerivedFrom befree-20140225 NP353267.RANJc_UIp-_65-Kp4JIrGfR4OFzSsKNRY2cqVMYOTtcnU130_provenance.
- NP353267.RANJc_UIp-_65-Kp4JIrGfR4OFzSsKNRY2cqVMYOTtcnU130_assertion wasGeneratedBy ECO_0000203 NP353267.RANJc_UIp-_65-Kp4JIrGfR4OFzSsKNRY2cqVMYOTtcnU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP353267.RANJc_UIp-_65-Kp4JIrGfR4OFzSsKNRY2cqVMYOTtcnU130_provenance.