Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1411404.RACgvXnknmvJBIQzx9-EJGCNjPMO5_EhJJyxU_ZboUSPw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1411404.RACgvXnknmvJBIQzx9-EJGCNjPMO5_EhJJyxU_ZboUSPw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1411404.RACgvXnknmvJBIQzx9-EJGCNjPMO5_EhJJyxU_ZboUSPw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1411404.RACgvXnknmvJBIQzx9-EJGCNjPMO5_EhJJyxU_ZboUSPw130_provenance.
- NP1411404.RACgvXnknmvJBIQzx9-EJGCNjPMO5_EhJJyxU_ZboUSPw130_assertion description "[In hereditary cystatin C amyloid angiopathy (HCCAA), presence of the Leu68 --> Gln substitution in cystatin C is coupled to a decreased concentration of this major cysteine proteinase inhibitor in cerebrospinal fluid and leads to its amyloid deposition in the brain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1411404.RACgvXnknmvJBIQzx9-EJGCNjPMO5_EhJJyxU_ZboUSPw130_provenance.
- NP1411404.RACgvXnknmvJBIQzx9-EJGCNjPMO5_EhJJyxU_ZboUSPw130_assertion evidence source_evidence_literature NP1411404.RACgvXnknmvJBIQzx9-EJGCNjPMO5_EhJJyxU_ZboUSPw130_provenance.
- NP1411404.RACgvXnknmvJBIQzx9-EJGCNjPMO5_EhJJyxU_ZboUSPw130_assertion SIO_000772 9860845 NP1411404.RACgvXnknmvJBIQzx9-EJGCNjPMO5_EhJJyxU_ZboUSPw130_provenance.
- NP1411404.RACgvXnknmvJBIQzx9-EJGCNjPMO5_EhJJyxU_ZboUSPw130_assertion wasDerivedFrom befree-2016 NP1411404.RACgvXnknmvJBIQzx9-EJGCNjPMO5_EhJJyxU_ZboUSPw130_provenance.
- NP1411404.RACgvXnknmvJBIQzx9-EJGCNjPMO5_EhJJyxU_ZboUSPw130_assertion wasGeneratedBy ECO_0000203 NP1411404.RACgvXnknmvJBIQzx9-EJGCNjPMO5_EhJJyxU_ZboUSPw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1411404.RACgvXnknmvJBIQzx9-EJGCNjPMO5_EhJJyxU_ZboUSPw130_provenance.