Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP25580.RA82lKkU1PC_zxHoRhWKB_o1EZFrxfqrike6DBcvc6Lso130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP25580.RA82lKkU1PC_zxHoRhWKB_o1EZFrxfqrike6DBcvc6Lso130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP25580.RA82lKkU1PC_zxHoRhWKB_o1EZFrxfqrike6DBcvc6Lso130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP25580.RA82lKkU1PC_zxHoRhWKB_o1EZFrxfqrike6DBcvc6Lso130_provenance.
- NP25580.RA82lKkU1PC_zxHoRhWKB_o1EZFrxfqrike6DBcvc6Lso130_assertion description "[Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP25580.RA82lKkU1PC_zxHoRhWKB_o1EZFrxfqrike6DBcvc6Lso130_provenance.
- NP25580.RA82lKkU1PC_zxHoRhWKB_o1EZFrxfqrike6DBcvc6Lso130_assertion evidence source_evidence_curated NP25580.RA82lKkU1PC_zxHoRhWKB_o1EZFrxfqrike6DBcvc6Lso130_provenance.
- NP25580.RA82lKkU1PC_zxHoRhWKB_o1EZFrxfqrike6DBcvc6Lso130_assertion SIO_000772 9539740 NP25580.RA82lKkU1PC_zxHoRhWKB_o1EZFrxfqrike6DBcvc6Lso130_provenance.
- NP25580.RA82lKkU1PC_zxHoRhWKB_o1EZFrxfqrike6DBcvc6Lso130_assertion wasDerivedFrom ctd_human-20150221 NP25580.RA82lKkU1PC_zxHoRhWKB_o1EZFrxfqrike6DBcvc6Lso130_provenance.
- NP25580.RA82lKkU1PC_zxHoRhWKB_o1EZFrxfqrike6DBcvc6Lso130_assertion wasGeneratedBy ECO_0000218 NP25580.RA82lKkU1PC_zxHoRhWKB_o1EZFrxfqrike6DBcvc6Lso130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP25580.RA82lKkU1PC_zxHoRhWKB_o1EZFrxfqrike6DBcvc6Lso130_provenance.