Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP817164.RABKkD3vDU-nJODv2IDxl_V8Pb6DZL4kcB8hlSLFO01ks130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP817164.RABKkD3vDU-nJODv2IDxl_V8Pb6DZL4kcB8hlSLFO01ks130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP817164.RABKkD3vDU-nJODv2IDxl_V8Pb6DZL4kcB8hlSLFO01ks130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP817164.RABKkD3vDU-nJODv2IDxl_V8Pb6DZL4kcB8hlSLFO01ks130_provenance.
- NP817164.RABKkD3vDU-nJODv2IDxl_V8Pb6DZL4kcB8hlSLFO01ks130_assertion description "[A mutation in SLC24A1 implicated in autosomal-recessive congenital stationary night blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP817164.RABKkD3vDU-nJODv2IDxl_V8Pb6DZL4kcB8hlSLFO01ks130_provenance.
- NP817164.RABKkD3vDU-nJODv2IDxl_V8Pb6DZL4kcB8hlSLFO01ks130_assertion evidence source_evidence_literature NP817164.RABKkD3vDU-nJODv2IDxl_V8Pb6DZL4kcB8hlSLFO01ks130_provenance.
- NP817164.RABKkD3vDU-nJODv2IDxl_V8Pb6DZL4kcB8hlSLFO01ks130_assertion SIO_000772 20850105 NP817164.RABKkD3vDU-nJODv2IDxl_V8Pb6DZL4kcB8hlSLFO01ks130_provenance.
- NP817164.RABKkD3vDU-nJODv2IDxl_V8Pb6DZL4kcB8hlSLFO01ks130_assertion wasDerivedFrom befree-20150227 NP817164.RABKkD3vDU-nJODv2IDxl_V8Pb6DZL4kcB8hlSLFO01ks130_provenance.
- NP817164.RABKkD3vDU-nJODv2IDxl_V8Pb6DZL4kcB8hlSLFO01ks130_assertion wasGeneratedBy ECO_0000203 NP817164.RABKkD3vDU-nJODv2IDxl_V8Pb6DZL4kcB8hlSLFO01ks130_provenance.
- befree-20150227 importedOn "2015-02-27" NP817164.RABKkD3vDU-nJODv2IDxl_V8Pb6DZL4kcB8hlSLFO01ks130_provenance.