Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP393.RAqiSEmUrZoY3S6vrpP6ti-pP3hlNVYYuo7ngvWbAJERs130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP393.RAqiSEmUrZoY3S6vrpP6ti-pP3hlNVYYuo7ngvWbAJERs130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP393.RAqiSEmUrZoY3S6vrpP6ti-pP3hlNVYYuo7ngvWbAJERs130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP393.RAqiSEmUrZoY3S6vrpP6ti-pP3hlNVYYuo7ngvWbAJERs130_provenance.
- NP393.RAqiSEmUrZoY3S6vrpP6ti-pP3hlNVYYuo7ngvWbAJERs130_assertion description "[Low frequency of ankyrin mutations in hereditary spherocytosis: identification of three novel mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP393.RAqiSEmUrZoY3S6vrpP6ti-pP3hlNVYYuo7ngvWbAJERs130_provenance.
- NP393.RAqiSEmUrZoY3S6vrpP6ti-pP3hlNVYYuo7ngvWbAJERs130_assertion evidence source_evidence_curated NP393.RAqiSEmUrZoY3S6vrpP6ti-pP3hlNVYYuo7ngvWbAJERs130_provenance.
- NP393.RAqiSEmUrZoY3S6vrpP6ti-pP3hlNVYYuo7ngvWbAJERs130_assertion SIO_000772 11102985 NP393.RAqiSEmUrZoY3S6vrpP6ti-pP3hlNVYYuo7ngvWbAJERs130_provenance.
- NP393.RAqiSEmUrZoY3S6vrpP6ti-pP3hlNVYYuo7ngvWbAJERs130_assertion wasDerivedFrom uniprot-20130724 NP393.RAqiSEmUrZoY3S6vrpP6ti-pP3hlNVYYuo7ngvWbAJERs130_provenance.
- NP393.RAqiSEmUrZoY3S6vrpP6ti-pP3hlNVYYuo7ngvWbAJERs130_assertion wasGeneratedBy ECO_0000218 NP393.RAqiSEmUrZoY3S6vrpP6ti-pP3hlNVYYuo7ngvWbAJERs130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP393.RAqiSEmUrZoY3S6vrpP6ti-pP3hlNVYYuo7ngvWbAJERs130_provenance.