Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP7293.RAWx1n6RFPZM88pnQtD0ur0gDOqFKhRW8scFOkbuzePyg130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP7293.RAWx1n6RFPZM88pnQtD0ur0gDOqFKhRW8scFOkbuzePyg130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP7293.RAWx1n6RFPZM88pnQtD0ur0gDOqFKhRW8scFOkbuzePyg130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP7293.RAWx1n6RFPZM88pnQtD0ur0gDOqFKhRW8scFOkbuzePyg130_provenance.
- NP7293.RAWx1n6RFPZM88pnQtD0ur0gDOqFKhRW8scFOkbuzePyg130_assertion description "[These studies open up the possibility that all PH1 mutations, which segregate with the minor allele, might also lead to the peroxisome-to-mitochondrion mistargeting of AGT, a suggestion that has important implications for the development of treatment strategies for PH1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7293.RAWx1n6RFPZM88pnQtD0ur0gDOqFKhRW8scFOkbuzePyg130_provenance.
- NP7293.RAWx1n6RFPZM88pnQtD0ur0gDOqFKhRW8scFOkbuzePyg130_assertion evidence source_evidence_curated NP7293.RAWx1n6RFPZM88pnQtD0ur0gDOqFKhRW8scFOkbuzePyg130_provenance.
- NP7293.RAWx1n6RFPZM88pnQtD0ur0gDOqFKhRW8scFOkbuzePyg130_assertion SIO_000772 23229545 NP7293.RAWx1n6RFPZM88pnQtD0ur0gDOqFKhRW8scFOkbuzePyg130_provenance.
- NP7293.RAWx1n6RFPZM88pnQtD0ur0gDOqFKhRW8scFOkbuzePyg130_assertion wasDerivedFrom uniprot-2016 NP7293.RAWx1n6RFPZM88pnQtD0ur0gDOqFKhRW8scFOkbuzePyg130_provenance.
- NP7293.RAWx1n6RFPZM88pnQtD0ur0gDOqFKhRW8scFOkbuzePyg130_assertion wasGeneratedBy ECO_0000218 NP7293.RAWx1n6RFPZM88pnQtD0ur0gDOqFKhRW8scFOkbuzePyg130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP7293.RAWx1n6RFPZM88pnQtD0ur0gDOqFKhRW8scFOkbuzePyg130_provenance.