Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP765728.RAyk134p_HzbtQTqTfIXxGVi-c68_PfZaeyIRHU7AR-Dg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP765728.RAyk134p_HzbtQTqTfIXxGVi-c68_PfZaeyIRHU7AR-Dg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP765728.RAyk134p_HzbtQTqTfIXxGVi-c68_PfZaeyIRHU7AR-Dg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP765728.RAyk134p_HzbtQTqTfIXxGVi-c68_PfZaeyIRHU7AR-Dg130_provenance.
- NP765728.RAyk134p_HzbtQTqTfIXxGVi-c68_PfZaeyIRHU7AR-Dg130_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." NP765728.RAyk134p_HzbtQTqTfIXxGVi-c68_PfZaeyIRHU7AR-Dg130_provenance.
- NP765728.RAyk134p_HzbtQTqTfIXxGVi-c68_PfZaeyIRHU7AR-Dg130_assertion evidence source_evidence_literature NP765728.RAyk134p_HzbtQTqTfIXxGVi-c68_PfZaeyIRHU7AR-Dg130_provenance.
- NP765728.RAyk134p_HzbtQTqTfIXxGVi-c68_PfZaeyIRHU7AR-Dg130_assertion SIO_000772 16097850 NP765728.RAyk134p_HzbtQTqTfIXxGVi-c68_PfZaeyIRHU7AR-Dg130_provenance.
- NP765728.RAyk134p_HzbtQTqTfIXxGVi-c68_PfZaeyIRHU7AR-Dg130_assertion wasDerivedFrom befree-20140225 NP765728.RAyk134p_HzbtQTqTfIXxGVi-c68_PfZaeyIRHU7AR-Dg130_provenance.
- NP765728.RAyk134p_HzbtQTqTfIXxGVi-c68_PfZaeyIRHU7AR-Dg130_assertion wasGeneratedBy ECO_0000203 NP765728.RAyk134p_HzbtQTqTfIXxGVi-c68_PfZaeyIRHU7AR-Dg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP765728.RAyk134p_HzbtQTqTfIXxGVi-c68_PfZaeyIRHU7AR-Dg130_provenance.