Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP935641.RAgzqlqXkC5R_kq-Sx2NVEUQde8haEHE5qSsu9mxs2CcI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP935641.RAgzqlqXkC5R_kq-Sx2NVEUQde8haEHE5qSsu9mxs2CcI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP935641.RAgzqlqXkC5R_kq-Sx2NVEUQde8haEHE5qSsu9mxs2CcI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP935641.RAgzqlqXkC5R_kq-Sx2NVEUQde8haEHE5qSsu9mxs2CcI130_provenance.
- NP935641.RAgzqlqXkC5R_kq-Sx2NVEUQde8haEHE5qSsu9mxs2CcI130_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." NP935641.RAgzqlqXkC5R_kq-Sx2NVEUQde8haEHE5qSsu9mxs2CcI130_provenance.
- NP935641.RAgzqlqXkC5R_kq-Sx2NVEUQde8haEHE5qSsu9mxs2CcI130_assertion evidence source_evidence_literature NP935641.RAgzqlqXkC5R_kq-Sx2NVEUQde8haEHE5qSsu9mxs2CcI130_provenance.
- NP935641.RAgzqlqXkC5R_kq-Sx2NVEUQde8haEHE5qSsu9mxs2CcI130_assertion SIO_000772 2900981 NP935641.RAgzqlqXkC5R_kq-Sx2NVEUQde8haEHE5qSsu9mxs2CcI130_provenance.
- NP935641.RAgzqlqXkC5R_kq-Sx2NVEUQde8haEHE5qSsu9mxs2CcI130_assertion wasDerivedFrom befree-20140225 NP935641.RAgzqlqXkC5R_kq-Sx2NVEUQde8haEHE5qSsu9mxs2CcI130_provenance.
- NP935641.RAgzqlqXkC5R_kq-Sx2NVEUQde8haEHE5qSsu9mxs2CcI130_assertion wasGeneratedBy ECO_0000203 NP935641.RAgzqlqXkC5R_kq-Sx2NVEUQde8haEHE5qSsu9mxs2CcI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP935641.RAgzqlqXkC5R_kq-Sx2NVEUQde8haEHE5qSsu9mxs2CcI130_provenance.