Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP856481.RAT6HIoE378HGlaABYIj6NKuPZ0PRxZl576zlhHk74u5s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP856481.RAT6HIoE378HGlaABYIj6NKuPZ0PRxZl576zlhHk74u5s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP856481.RAT6HIoE378HGlaABYIj6NKuPZ0PRxZl576zlhHk74u5s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP856481.RAT6HIoE378HGlaABYIj6NKuPZ0PRxZl576zlhHk74u5s130_provenance.
- NP856481.RAT6HIoE378HGlaABYIj6NKuPZ0PRxZl576zlhHk74u5s130_assertion description "[These findings expand the phenotype associated with AFG3L2 mutations and suggest that AFG3L2-related disease should be considered in the differential diagnosis of spastic ataxias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP856481.RAT6HIoE378HGlaABYIj6NKuPZ0PRxZl576zlhHk74u5s130_provenance.
- NP856481.RAT6HIoE378HGlaABYIj6NKuPZ0PRxZl576zlhHk74u5s130_assertion evidence source_evidence_literature NP856481.RAT6HIoE378HGlaABYIj6NKuPZ0PRxZl576zlhHk74u5s130_provenance.
- NP856481.RAT6HIoE378HGlaABYIj6NKuPZ0PRxZl576zlhHk74u5s130_assertion SIO_000772 22022284 NP856481.RAT6HIoE378HGlaABYIj6NKuPZ0PRxZl576zlhHk74u5s130_provenance.
- NP856481.RAT6HIoE378HGlaABYIj6NKuPZ0PRxZl576zlhHk74u5s130_assertion wasDerivedFrom befree-20150227 NP856481.RAT6HIoE378HGlaABYIj6NKuPZ0PRxZl576zlhHk74u5s130_provenance.
- NP856481.RAT6HIoE378HGlaABYIj6NKuPZ0PRxZl576zlhHk74u5s130_assertion wasGeneratedBy ECO_0000203 NP856481.RAT6HIoE378HGlaABYIj6NKuPZ0PRxZl576zlhHk74u5s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP856481.RAT6HIoE378HGlaABYIj6NKuPZ0PRxZl576zlhHk74u5s130_provenance.