Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP859803.RANXLy-2euuGtVwpSsm7jfpCex8aroULXcWMc6BpT9Ms0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP859803.RANXLy-2euuGtVwpSsm7jfpCex8aroULXcWMc6BpT9Ms0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP859803.RANXLy-2euuGtVwpSsm7jfpCex8aroULXcWMc6BpT9Ms0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP859803.RANXLy-2euuGtVwpSsm7jfpCex8aroULXcWMc6BpT9Ms0130_provenance.
- NP859803.RANXLy-2euuGtVwpSsm7jfpCex8aroULXcWMc6BpT9Ms0130_assertion description "[Mutations in the peripherin/RDS gene have been identified in families with various retinopathies including those affecting primarily the macula and those restricted to the retinal periphery.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP859803.RANXLy-2euuGtVwpSsm7jfpCex8aroULXcWMc6BpT9Ms0130_provenance.
- NP859803.RANXLy-2euuGtVwpSsm7jfpCex8aroULXcWMc6BpT9Ms0130_assertion evidence source_evidence_literature NP859803.RANXLy-2euuGtVwpSsm7jfpCex8aroULXcWMc6BpT9Ms0130_provenance.
- NP859803.RANXLy-2euuGtVwpSsm7jfpCex8aroULXcWMc6BpT9Ms0130_assertion SIO_000772 17148040 NP859803.RANXLy-2euuGtVwpSsm7jfpCex8aroULXcWMc6BpT9Ms0130_provenance.
- NP859803.RANXLy-2euuGtVwpSsm7jfpCex8aroULXcWMc6BpT9Ms0130_assertion wasDerivedFrom befree-20140225 NP859803.RANXLy-2euuGtVwpSsm7jfpCex8aroULXcWMc6BpT9Ms0130_provenance.
- NP859803.RANXLy-2euuGtVwpSsm7jfpCex8aroULXcWMc6BpT9Ms0130_assertion wasGeneratedBy ECO_0000203 NP859803.RANXLy-2euuGtVwpSsm7jfpCex8aroULXcWMc6BpT9Ms0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP859803.RANXLy-2euuGtVwpSsm7jfpCex8aroULXcWMc6BpT9Ms0130_provenance.