Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP586029.RA3z5xy62JcFULfmlShJuqEQCKiX8NTsVFgEYhUGnRGSw130_assertion> ?p ?o ?g. }
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- NP586029.RA3z5xy62JcFULfmlShJuqEQCKiX8NTsVFgEYhUGnRGSw130_assertion type Assertion NP586029.RA3z5xy62JcFULfmlShJuqEQCKiX8NTsVFgEYhUGnRGSw130_head.
- NP586029.RA3z5xy62JcFULfmlShJuqEQCKiX8NTsVFgEYhUGnRGSw130_assertion description "[Hereditary conditions, including CADASIL (cerebral autosomal dominant arteriopathy with sub-cortical infarcts and leukoencephalopathy), MELAS (mitochondrial myopathy, encephalopathy, lactacidosis and stroke) and hereditary haemorrhagic telangiectasia, appear to predispose to both migraine and stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP586029.RA3z5xy62JcFULfmlShJuqEQCKiX8NTsVFgEYhUGnRGSw130_provenance.
- NP586029.RA3z5xy62JcFULfmlShJuqEQCKiX8NTsVFgEYhUGnRGSw130_assertion evidence source_evidence_literature NP586029.RA3z5xy62JcFULfmlShJuqEQCKiX8NTsVFgEYhUGnRGSw130_provenance.
- NP586029.RA3z5xy62JcFULfmlShJuqEQCKiX8NTsVFgEYhUGnRGSw130_assertion SIO_000772 16097850 NP586029.RA3z5xy62JcFULfmlShJuqEQCKiX8NTsVFgEYhUGnRGSw130_provenance.
- NP586029.RA3z5xy62JcFULfmlShJuqEQCKiX8NTsVFgEYhUGnRGSw130_assertion wasDerivedFrom befree-20140225 NP586029.RA3z5xy62JcFULfmlShJuqEQCKiX8NTsVFgEYhUGnRGSw130_provenance.
- NP586029.RA3z5xy62JcFULfmlShJuqEQCKiX8NTsVFgEYhUGnRGSw130_assertion wasGeneratedBy ECO_0000203 NP586029.RA3z5xy62JcFULfmlShJuqEQCKiX8NTsVFgEYhUGnRGSw130_provenance.