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- source_evidence_literature type ECO_0000212 NP1298182.RAQ4dJ3sfXQ-x9pgWDwaWhTNU1BQSJvGiJhhhrJnFkr74130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1298182.RAQ4dJ3sfXQ-x9pgWDwaWhTNU1BQSJvGiJhhhrJnFkr74130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1298182.RAQ4dJ3sfXQ-x9pgWDwaWhTNU1BQSJvGiJhhhrJnFkr74130_provenance.
- NP1298182.RAQ4dJ3sfXQ-x9pgWDwaWhTNU1BQSJvGiJhhhrJnFkr74130_assertion description "[Hereditary cystatin C amyloid angiopathy (HCCAA) is an autosomal dominant disorder in which a cysteine proteinase inhibitor, cystatin C, is deposited as amyloid fibrils in the cerebral arteries of patients and leads to massive brain haemorrhage and death in young adults.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1298182.RAQ4dJ3sfXQ-x9pgWDwaWhTNU1BQSJvGiJhhhrJnFkr74130_provenance.
- NP1298182.RAQ4dJ3sfXQ-x9pgWDwaWhTNU1BQSJvGiJhhhrJnFkr74130_assertion evidence source_evidence_literature NP1298182.RAQ4dJ3sfXQ-x9pgWDwaWhTNU1BQSJvGiJhhhrJnFkr74130_provenance.
- NP1298182.RAQ4dJ3sfXQ-x9pgWDwaWhTNU1BQSJvGiJhhhrJnFkr74130_assertion SIO_000772 2900981 NP1298182.RAQ4dJ3sfXQ-x9pgWDwaWhTNU1BQSJvGiJhhhrJnFkr74130_provenance.
- NP1298182.RAQ4dJ3sfXQ-x9pgWDwaWhTNU1BQSJvGiJhhhrJnFkr74130_assertion wasDerivedFrom befree-2016 NP1298182.RAQ4dJ3sfXQ-x9pgWDwaWhTNU1BQSJvGiJhhhrJnFkr74130_provenance.
- NP1298182.RAQ4dJ3sfXQ-x9pgWDwaWhTNU1BQSJvGiJhhhrJnFkr74130_assertion wasGeneratedBy ECO_0000203 NP1298182.RAQ4dJ3sfXQ-x9pgWDwaWhTNU1BQSJvGiJhhhrJnFkr74130_provenance.
- befree-2016 importedOn "2016-02-19" NP1298182.RAQ4dJ3sfXQ-x9pgWDwaWhTNU1BQSJvGiJhhhrJnFkr74130_provenance.