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- source_evidence_literature type ECO_0000212 NP1211366.RA83NS91JTyZV20fyp69F_nTALxl9TFQt9j1w7y-uuVtE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1211366.RA83NS91JTyZV20fyp69F_nTALxl9TFQt9j1w7y-uuVtE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1211366.RA83NS91JTyZV20fyp69F_nTALxl9TFQt9j1w7y-uuVtE130_provenance.
- NP1211366.RA83NS91JTyZV20fyp69F_nTALxl9TFQt9j1w7y-uuVtE130_assertion description "[The results suggested that the LOXL1 variants, which are well-established markers for EX, are not likely genetic markers for CRVO in Japanese subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1211366.RA83NS91JTyZV20fyp69F_nTALxl9TFQt9j1w7y-uuVtE130_provenance.
- NP1211366.RA83NS91JTyZV20fyp69F_nTALxl9TFQt9j1w7y-uuVtE130_assertion evidence source_evidence_literature NP1211366.RA83NS91JTyZV20fyp69F_nTALxl9TFQt9j1w7y-uuVtE130_provenance.
- NP1211366.RA83NS91JTyZV20fyp69F_nTALxl9TFQt9j1w7y-uuVtE130_assertion SIO_000772 25130441 NP1211366.RA83NS91JTyZV20fyp69F_nTALxl9TFQt9j1w7y-uuVtE130_provenance.
- NP1211366.RA83NS91JTyZV20fyp69F_nTALxl9TFQt9j1w7y-uuVtE130_assertion wasDerivedFrom befree-2016 NP1211366.RA83NS91JTyZV20fyp69F_nTALxl9TFQt9j1w7y-uuVtE130_provenance.
- NP1211366.RA83NS91JTyZV20fyp69F_nTALxl9TFQt9j1w7y-uuVtE130_assertion wasGeneratedBy ECO_0000203 NP1211366.RA83NS91JTyZV20fyp69F_nTALxl9TFQt9j1w7y-uuVtE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1211366.RA83NS91JTyZV20fyp69F_nTALxl9TFQt9j1w7y-uuVtE130_provenance.