Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP164681.RAcUsahWTZx1cUPf5SncNocIuhx52fUFXdHEGVts-jTY0130_assertion> ?p ?o ?g. }
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- NP164681.RAcUsahWTZx1cUPf5SncNocIuhx52fUFXdHEGVts-jTY0130_assertion type Assertion NP164681.RAcUsahWTZx1cUPf5SncNocIuhx52fUFXdHEGVts-jTY0130_head.
- NP164681.RAcUsahWTZx1cUPf5SncNocIuhx52fUFXdHEGVts-jTY0130_assertion description "[Screening for these polymorphisms would probably constitute a valuable procedure in N-AION patients, as they may have an important contribution to the pathogenesis of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP164681.RAcUsahWTZx1cUPf5SncNocIuhx52fUFXdHEGVts-jTY0130_provenance.
- NP164681.RAcUsahWTZx1cUPf5SncNocIuhx52fUFXdHEGVts-jTY0130_assertion evidence source_evidence_literature NP164681.RAcUsahWTZx1cUPf5SncNocIuhx52fUFXdHEGVts-jTY0130_provenance.
- NP164681.RAcUsahWTZx1cUPf5SncNocIuhx52fUFXdHEGVts-jTY0130_assertion SIO_000772 20162297 NP164681.RAcUsahWTZx1cUPf5SncNocIuhx52fUFXdHEGVts-jTY0130_provenance.
- NP164681.RAcUsahWTZx1cUPf5SncNocIuhx52fUFXdHEGVts-jTY0130_assertion wasDerivedFrom gad-20150221 NP164681.RAcUsahWTZx1cUPf5SncNocIuhx52fUFXdHEGVts-jTY0130_provenance.
- NP164681.RAcUsahWTZx1cUPf5SncNocIuhx52fUFXdHEGVts-jTY0130_assertion wasGeneratedBy ECO_0000203 NP164681.RAcUsahWTZx1cUPf5SncNocIuhx52fUFXdHEGVts-jTY0130_provenance.