Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1081.RAj2XwMnt9difsbZGNJ7CvZTLT3_PrAGNCNxefPD8TWg0130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP1081.RAj2XwMnt9difsbZGNJ7CvZTLT3_PrAGNCNxefPD8TWg0130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1081.RAj2XwMnt9difsbZGNJ7CvZTLT3_PrAGNCNxefPD8TWg0130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1081.RAj2XwMnt9difsbZGNJ7CvZTLT3_PrAGNCNxefPD8TWg0130_provenance.
- NP1081.RAj2XwMnt9difsbZGNJ7CvZTLT3_PrAGNCNxefPD8TWg0130_assertion description "[Hereditary myeloperoxidase (MPO) deficiency is a neutrophil disorder characterized by the lack of peroxidase activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1081.RAj2XwMnt9difsbZGNJ7CvZTLT3_PrAGNCNxefPD8TWg0130_provenance.
- NP1081.RAj2XwMnt9difsbZGNJ7CvZTLT3_PrAGNCNxefPD8TWg0130_assertion evidence source_evidence_curated NP1081.RAj2XwMnt9difsbZGNJ7CvZTLT3_PrAGNCNxefPD8TWg0130_provenance.
- NP1081.RAj2XwMnt9difsbZGNJ7CvZTLT3_PrAGNCNxefPD8TWg0130_assertion SIO_000772 9354683 NP1081.RAj2XwMnt9difsbZGNJ7CvZTLT3_PrAGNCNxefPD8TWg0130_provenance.
- NP1081.RAj2XwMnt9difsbZGNJ7CvZTLT3_PrAGNCNxefPD8TWg0130_assertion wasDerivedFrom uniprot-20150221 NP1081.RAj2XwMnt9difsbZGNJ7CvZTLT3_PrAGNCNxefPD8TWg0130_provenance.
- NP1081.RAj2XwMnt9difsbZGNJ7CvZTLT3_PrAGNCNxefPD8TWg0130_assertion wasGeneratedBy ECO_0000218 NP1081.RAj2XwMnt9difsbZGNJ7CvZTLT3_PrAGNCNxefPD8TWg0130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP1081.RAj2XwMnt9difsbZGNJ7CvZTLT3_PrAGNCNxefPD8TWg0130_provenance.