Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1368518.RAYzavcmoXc9ShDg8Q3--Ys3gMwcX8c_j92g8tOTfQBws130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1368518.RAYzavcmoXc9ShDg8Q3--Ys3gMwcX8c_j92g8tOTfQBws130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1368518.RAYzavcmoXc9ShDg8Q3--Ys3gMwcX8c_j92g8tOTfQBws130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1368518.RAYzavcmoXc9ShDg8Q3--Ys3gMwcX8c_j92g8tOTfQBws130_provenance.
- NP1368518.RAYzavcmoXc9ShDg8Q3--Ys3gMwcX8c_j92g8tOTfQBws130_assertion description "[Stargardt disease (STGD, also known as fundus flavimaculatus; FFM) is an autosomal recessive retinal disorder characterized by a juvenile-onset macular dystrophy, alterations of the peripheral retina, and subretinal deposition of lipofuscin-like material.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1368518.RAYzavcmoXc9ShDg8Q3--Ys3gMwcX8c_j92g8tOTfQBws130_provenance.
- NP1368518.RAYzavcmoXc9ShDg8Q3--Ys3gMwcX8c_j92g8tOTfQBws130_assertion evidence source_evidence_literature NP1368518.RAYzavcmoXc9ShDg8Q3--Ys3gMwcX8c_j92g8tOTfQBws130_provenance.
- NP1368518.RAYzavcmoXc9ShDg8Q3--Ys3gMwcX8c_j92g8tOTfQBws130_assertion SIO_000772 9054934 NP1368518.RAYzavcmoXc9ShDg8Q3--Ys3gMwcX8c_j92g8tOTfQBws130_provenance.
- NP1368518.RAYzavcmoXc9ShDg8Q3--Ys3gMwcX8c_j92g8tOTfQBws130_assertion wasDerivedFrom befree-2016 NP1368518.RAYzavcmoXc9ShDg8Q3--Ys3gMwcX8c_j92g8tOTfQBws130_provenance.
- NP1368518.RAYzavcmoXc9ShDg8Q3--Ys3gMwcX8c_j92g8tOTfQBws130_assertion wasGeneratedBy ECO_0000203 NP1368518.RAYzavcmoXc9ShDg8Q3--Ys3gMwcX8c_j92g8tOTfQBws130_provenance.
- befree-2016 importedOn "2016-02-19" NP1368518.RAYzavcmoXc9ShDg8Q3--Ys3gMwcX8c_j92g8tOTfQBws130_provenance.