Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP205185.RAFGK6O-XloHdEUp2ruSL6PJgL3iPgFk3fDpDLiFO5ARg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP205185.RAFGK6O-XloHdEUp2ruSL6PJgL3iPgFk3fDpDLiFO5ARg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP205185.RAFGK6O-XloHdEUp2ruSL6PJgL3iPgFk3fDpDLiFO5ARg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP205185.RAFGK6O-XloHdEUp2ruSL6PJgL3iPgFk3fDpDLiFO5ARg130_provenance.
- NP205185.RAFGK6O-XloHdEUp2ruSL6PJgL3iPgFk3fDpDLiFO5ARg130_assertion description "[The 12 carriers of XLRP had a spectrum of fundus abnormalities and varying severity of functional impairment as derived from visual field areas and ERG amplitudes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205185.RAFGK6O-XloHdEUp2ruSL6PJgL3iPgFk3fDpDLiFO5ARg130_provenance.
- NP205185.RAFGK6O-XloHdEUp2ruSL6PJgL3iPgFk3fDpDLiFO5ARg130_assertion evidence source_evidence_literature NP205185.RAFGK6O-XloHdEUp2ruSL6PJgL3iPgFk3fDpDLiFO5ARg130_provenance.
- NP205185.RAFGK6O-XloHdEUp2ruSL6PJgL3iPgFk3fDpDLiFO5ARg130_assertion SIO_000772 11772598 NP205185.RAFGK6O-XloHdEUp2ruSL6PJgL3iPgFk3fDpDLiFO5ARg130_provenance.
- NP205185.RAFGK6O-XloHdEUp2ruSL6PJgL3iPgFk3fDpDLiFO5ARg130_assertion wasDerivedFrom befree-20140225 NP205185.RAFGK6O-XloHdEUp2ruSL6PJgL3iPgFk3fDpDLiFO5ARg130_provenance.
- NP205185.RAFGK6O-XloHdEUp2ruSL6PJgL3iPgFk3fDpDLiFO5ARg130_assertion wasGeneratedBy ECO_0000203 NP205185.RAFGK6O-XloHdEUp2ruSL6PJgL3iPgFk3fDpDLiFO5ARg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP205185.RAFGK6O-XloHdEUp2ruSL6PJgL3iPgFk3fDpDLiFO5ARg130_provenance.