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- source_evidence_literature type ECO_0000212 NP854771.RA17cW0FGBx4hcuf8CkejD6fXSo66RehmIaROpqaH39A0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP854771.RA17cW0FGBx4hcuf8CkejD6fXSo66RehmIaROpqaH39A0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP854771.RA17cW0FGBx4hcuf8CkejD6fXSo66RehmIaROpqaH39A0130_provenance.
- NP854771.RA17cW0FGBx4hcuf8CkejD6fXSo66RehmIaROpqaH39A0130_assertion description "[Copy number variations in regulators of complement activation genes (CFHR1 and CFHR3) and glutathione S transferase genes (GSTM1 and GSTT1) have been associated with AMD, and several additional loci have been identified as regions of potential interest but require further evaluation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP854771.RA17cW0FGBx4hcuf8CkejD6fXSo66RehmIaROpqaH39A0130_provenance.
- NP854771.RA17cW0FGBx4hcuf8CkejD6fXSo66RehmIaROpqaH39A0130_assertion evidence source_evidence_literature NP854771.RA17cW0FGBx4hcuf8CkejD6fXSo66RehmIaROpqaH39A0130_provenance.
- NP854771.RA17cW0FGBx4hcuf8CkejD6fXSo66RehmIaROpqaH39A0130_assertion SIO_000772 23244519 NP854771.RA17cW0FGBx4hcuf8CkejD6fXSo66RehmIaROpqaH39A0130_provenance.
- NP854771.RA17cW0FGBx4hcuf8CkejD6fXSo66RehmIaROpqaH39A0130_assertion wasDerivedFrom befree-20150227 NP854771.RA17cW0FGBx4hcuf8CkejD6fXSo66RehmIaROpqaH39A0130_provenance.
- NP854771.RA17cW0FGBx4hcuf8CkejD6fXSo66RehmIaROpqaH39A0130_assertion wasGeneratedBy ECO_0000203 NP854771.RA17cW0FGBx4hcuf8CkejD6fXSo66RehmIaROpqaH39A0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP854771.RA17cW0FGBx4hcuf8CkejD6fXSo66RehmIaROpqaH39A0130_provenance.