Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP504979.RAHECnG5NOimSIrf2bY_LJ51pu_j0RclwFrykW19VYpU0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP504979.RAHECnG5NOimSIrf2bY_LJ51pu_j0RclwFrykW19VYpU0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP504979.RAHECnG5NOimSIrf2bY_LJ51pu_j0RclwFrykW19VYpU0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP504979.RAHECnG5NOimSIrf2bY_LJ51pu_j0RclwFrykW19VYpU0130_provenance.
- NP504979.RAHECnG5NOimSIrf2bY_LJ51pu_j0RclwFrykW19VYpU0130_assertion description "[Thus, although some atypical Norrie disease patients lack both MAO-A and MAO-B activities, MAO does not appear to be an etiologic factor in classic Norrie disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP504979.RAHECnG5NOimSIrf2bY_LJ51pu_j0RclwFrykW19VYpU0130_provenance.
- NP504979.RAHECnG5NOimSIrf2bY_LJ51pu_j0RclwFrykW19VYpU0130_assertion evidence source_evidence_literature NP504979.RAHECnG5NOimSIrf2bY_LJ51pu_j0RclwFrykW19VYpU0130_provenance.
- NP504979.RAHECnG5NOimSIrf2bY_LJ51pu_j0RclwFrykW19VYpU0130_assertion SIO_000772 2773935 NP504979.RAHECnG5NOimSIrf2bY_LJ51pu_j0RclwFrykW19VYpU0130_provenance.
- NP504979.RAHECnG5NOimSIrf2bY_LJ51pu_j0RclwFrykW19VYpU0130_assertion wasDerivedFrom befree-20140225 NP504979.RAHECnG5NOimSIrf2bY_LJ51pu_j0RclwFrykW19VYpU0130_provenance.
- NP504979.RAHECnG5NOimSIrf2bY_LJ51pu_j0RclwFrykW19VYpU0130_assertion wasGeneratedBy ECO_0000203 NP504979.RAHECnG5NOimSIrf2bY_LJ51pu_j0RclwFrykW19VYpU0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP504979.RAHECnG5NOimSIrf2bY_LJ51pu_j0RclwFrykW19VYpU0130_provenance.