Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP902022.RAGXXzN0EKImBvdmV4Gi-AGk7XRbuvQV3ve8xXNOPUa80130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP902022.RAGXXzN0EKImBvdmV4Gi-AGk7XRbuvQV3ve8xXNOPUa80130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP902022.RAGXXzN0EKImBvdmV4Gi-AGk7XRbuvQV3ve8xXNOPUa80130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP902022.RAGXXzN0EKImBvdmV4Gi-AGk7XRbuvQV3ve8xXNOPUa80130_provenance.
- NP902022.RAGXXzN0EKImBvdmV4Gi-AGk7XRbuvQV3ve8xXNOPUa80130_assertion description "[HSP is a genetically diverse group of disorders characterized by insidiously progressive spastic weakness in the legs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP902022.RAGXXzN0EKImBvdmV4Gi-AGk7XRbuvQV3ve8xXNOPUa80130_provenance.
- NP902022.RAGXXzN0EKImBvdmV4Gi-AGk7XRbuvQV3ve8xXNOPUa80130_assertion evidence source_evidence_literature NP902022.RAGXXzN0EKImBvdmV4Gi-AGk7XRbuvQV3ve8xXNOPUa80130_provenance.
- NP902022.RAGXXzN0EKImBvdmV4Gi-AGk7XRbuvQV3ve8xXNOPUa80130_assertion SIO_000772 10408535 NP902022.RAGXXzN0EKImBvdmV4Gi-AGk7XRbuvQV3ve8xXNOPUa80130_provenance.
- NP902022.RAGXXzN0EKImBvdmV4Gi-AGk7XRbuvQV3ve8xXNOPUa80130_assertion wasDerivedFrom befree-20140225 NP902022.RAGXXzN0EKImBvdmV4Gi-AGk7XRbuvQV3ve8xXNOPUa80130_provenance.
- NP902022.RAGXXzN0EKImBvdmV4Gi-AGk7XRbuvQV3ve8xXNOPUa80130_assertion wasGeneratedBy ECO_0000203 NP902022.RAGXXzN0EKImBvdmV4Gi-AGk7XRbuvQV3ve8xXNOPUa80130_provenance.
- befree-20140225 importedOn "2014-02-25" NP902022.RAGXXzN0EKImBvdmV4Gi-AGk7XRbuvQV3ve8xXNOPUa80130_provenance.