Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP384059.RAhWxlV5_oST3Xp_JYyI-jWJjcJ9SIQ4Hz_ehBHtVevtI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP384059.RAhWxlV5_oST3Xp_JYyI-jWJjcJ9SIQ4Hz_ehBHtVevtI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP384059.RAhWxlV5_oST3Xp_JYyI-jWJjcJ9SIQ4Hz_ehBHtVevtI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP384059.RAhWxlV5_oST3Xp_JYyI-jWJjcJ9SIQ4Hz_ehBHtVevtI130_provenance.
- NP384059.RAhWxlV5_oST3Xp_JYyI-jWJjcJ9SIQ4Hz_ehBHtVevtI130_assertion description "[To review three inherited retinal disorders associated with diagnostic or pathognomonic electroretinogram (ERG) abnormalities: cone dystrophy with supernormal rod ERG (KCNV2), enhanced S-cone syndrome (NR2E3), and bradyopsia (RGS9/R9AP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP384059.RAhWxlV5_oST3Xp_JYyI-jWJjcJ9SIQ4Hz_ehBHtVevtI130_provenance.
- NP384059.RAhWxlV5_oST3Xp_JYyI-jWJjcJ9SIQ4Hz_ehBHtVevtI130_assertion evidence source_evidence_literature NP384059.RAhWxlV5_oST3Xp_JYyI-jWJjcJ9SIQ4Hz_ehBHtVevtI130_provenance.
- NP384059.RAhWxlV5_oST3Xp_JYyI-jWJjcJ9SIQ4Hz_ehBHtVevtI130_assertion SIO_000772 23263253 NP384059.RAhWxlV5_oST3Xp_JYyI-jWJjcJ9SIQ4Hz_ehBHtVevtI130_provenance.
- NP384059.RAhWxlV5_oST3Xp_JYyI-jWJjcJ9SIQ4Hz_ehBHtVevtI130_assertion wasDerivedFrom befree-20140225 NP384059.RAhWxlV5_oST3Xp_JYyI-jWJjcJ9SIQ4Hz_ehBHtVevtI130_provenance.
- NP384059.RAhWxlV5_oST3Xp_JYyI-jWJjcJ9SIQ4Hz_ehBHtVevtI130_assertion wasGeneratedBy ECO_0000203 NP384059.RAhWxlV5_oST3Xp_JYyI-jWJjcJ9SIQ4Hz_ehBHtVevtI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP384059.RAhWxlV5_oST3Xp_JYyI-jWJjcJ9SIQ4Hz_ehBHtVevtI130_provenance.