Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP236382.RAlht_DT4BJr5mJnXn13AGcIJ29wLMLE_qoInTm7cAUoU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP236382.RAlht_DT4BJr5mJnXn13AGcIJ29wLMLE_qoInTm7cAUoU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP236382.RAlht_DT4BJr5mJnXn13AGcIJ29wLMLE_qoInTm7cAUoU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP236382.RAlht_DT4BJr5mJnXn13AGcIJ29wLMLE_qoInTm7cAUoU130_provenance.
- NP236382.RAlht_DT4BJr5mJnXn13AGcIJ29wLMLE_qoInTm7cAUoU130_assertion description "[The clinical course and typical ERG pattern indicated a 'cone dystrophy with supernormal rod electroretinogram' in the proband, and SD-OCT demonstrated a subfoveal optical gap with loss of the inner segment/outer segment junction line.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP236382.RAlht_DT4BJr5mJnXn13AGcIJ29wLMLE_qoInTm7cAUoU130_provenance.
- NP236382.RAlht_DT4BJr5mJnXn13AGcIJ29wLMLE_qoInTm7cAUoU130_assertion evidence source_evidence_literature NP236382.RAlht_DT4BJr5mJnXn13AGcIJ29wLMLE_qoInTm7cAUoU130_provenance.
- NP236382.RAlht_DT4BJr5mJnXn13AGcIJ29wLMLE_qoInTm7cAUoU130_assertion SIO_000772 23143909 NP236382.RAlht_DT4BJr5mJnXn13AGcIJ29wLMLE_qoInTm7cAUoU130_provenance.
- NP236382.RAlht_DT4BJr5mJnXn13AGcIJ29wLMLE_qoInTm7cAUoU130_assertion wasDerivedFrom befree-20140225 NP236382.RAlht_DT4BJr5mJnXn13AGcIJ29wLMLE_qoInTm7cAUoU130_provenance.
- NP236382.RAlht_DT4BJr5mJnXn13AGcIJ29wLMLE_qoInTm7cAUoU130_assertion wasGeneratedBy ECO_0000203 NP236382.RAlht_DT4BJr5mJnXn13AGcIJ29wLMLE_qoInTm7cAUoU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP236382.RAlht_DT4BJr5mJnXn13AGcIJ29wLMLE_qoInTm7cAUoU130_provenance.