Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP218847.RAOnwI5RUw4hyVM0Qv4dcKzjiQt4nYc3DjAY_IopUWH5I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP218847.RAOnwI5RUw4hyVM0Qv4dcKzjiQt4nYc3DjAY_IopUWH5I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP218847.RAOnwI5RUw4hyVM0Qv4dcKzjiQt4nYc3DjAY_IopUWH5I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP218847.RAOnwI5RUw4hyVM0Qv4dcKzjiQt4nYc3DjAY_IopUWH5I130_provenance.
- NP218847.RAOnwI5RUw4hyVM0Qv4dcKzjiQt4nYc3DjAY_IopUWH5I130_assertion description "[The retina-specific ATP binding cassette transporter, ABCA4 protein, is associated with a broad range of inherited macular degenerations, including Stargardt disease, autosomal recessive cone rod dystrophy, and fundus flavimaculatus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP218847.RAOnwI5RUw4hyVM0Qv4dcKzjiQt4nYc3DjAY_IopUWH5I130_provenance.
- NP218847.RAOnwI5RUw4hyVM0Qv4dcKzjiQt4nYc3DjAY_IopUWH5I130_assertion evidence source_evidence_literature NP218847.RAOnwI5RUw4hyVM0Qv4dcKzjiQt4nYc3DjAY_IopUWH5I130_provenance.
- NP218847.RAOnwI5RUw4hyVM0Qv4dcKzjiQt4nYc3DjAY_IopUWH5I130_assertion SIO_000772 23144455 NP218847.RAOnwI5RUw4hyVM0Qv4dcKzjiQt4nYc3DjAY_IopUWH5I130_provenance.
- NP218847.RAOnwI5RUw4hyVM0Qv4dcKzjiQt4nYc3DjAY_IopUWH5I130_assertion wasDerivedFrom befree-20150227 NP218847.RAOnwI5RUw4hyVM0Qv4dcKzjiQt4nYc3DjAY_IopUWH5I130_provenance.
- NP218847.RAOnwI5RUw4hyVM0Qv4dcKzjiQt4nYc3DjAY_IopUWH5I130_assertion wasGeneratedBy ECO_0000203 NP218847.RAOnwI5RUw4hyVM0Qv4dcKzjiQt4nYc3DjAY_IopUWH5I130_provenance.
- befree-20150227 importedOn "2015-02-27" NP218847.RAOnwI5RUw4hyVM0Qv4dcKzjiQt4nYc3DjAY_IopUWH5I130_provenance.