Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP647328.RA6SZ1OiDvgVGZopi5tT53xeFV2BdnDIHRNbkggQbeaP4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP647328.RA6SZ1OiDvgVGZopi5tT53xeFV2BdnDIHRNbkggQbeaP4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP647328.RA6SZ1OiDvgVGZopi5tT53xeFV2BdnDIHRNbkggQbeaP4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP647328.RA6SZ1OiDvgVGZopi5tT53xeFV2BdnDIHRNbkggQbeaP4130_provenance.
- NP647328.RA6SZ1OiDvgVGZopi5tT53xeFV2BdnDIHRNbkggQbeaP4130_assertion description "[Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP647328.RA6SZ1OiDvgVGZopi5tT53xeFV2BdnDIHRNbkggQbeaP4130_provenance.
- NP647328.RA6SZ1OiDvgVGZopi5tT53xeFV2BdnDIHRNbkggQbeaP4130_assertion evidence source_evidence_literature NP647328.RA6SZ1OiDvgVGZopi5tT53xeFV2BdnDIHRNbkggQbeaP4130_provenance.
- NP647328.RA6SZ1OiDvgVGZopi5tT53xeFV2BdnDIHRNbkggQbeaP4130_assertion SIO_000772 8570627 NP647328.RA6SZ1OiDvgVGZopi5tT53xeFV2BdnDIHRNbkggQbeaP4130_provenance.
- NP647328.RA6SZ1OiDvgVGZopi5tT53xeFV2BdnDIHRNbkggQbeaP4130_assertion wasDerivedFrom befree-20150227 NP647328.RA6SZ1OiDvgVGZopi5tT53xeFV2BdnDIHRNbkggQbeaP4130_provenance.
- NP647328.RA6SZ1OiDvgVGZopi5tT53xeFV2BdnDIHRNbkggQbeaP4130_assertion wasGeneratedBy ECO_0000203 NP647328.RA6SZ1OiDvgVGZopi5tT53xeFV2BdnDIHRNbkggQbeaP4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP647328.RA6SZ1OiDvgVGZopi5tT53xeFV2BdnDIHRNbkggQbeaP4130_provenance.