Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP424776.RAtBkQPcL0sAoed2hpkhYZpuH0D_z40FtlMTlwo3ULD_s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP424776.RAtBkQPcL0sAoed2hpkhYZpuH0D_z40FtlMTlwo3ULD_s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP424776.RAtBkQPcL0sAoed2hpkhYZpuH0D_z40FtlMTlwo3ULD_s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP424776.RAtBkQPcL0sAoed2hpkhYZpuH0D_z40FtlMTlwo3ULD_s130_provenance.
- NP424776.RAtBkQPcL0sAoed2hpkhYZpuH0D_z40FtlMTlwo3ULD_s130_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." NP424776.RAtBkQPcL0sAoed2hpkhYZpuH0D_z40FtlMTlwo3ULD_s130_provenance.
- NP424776.RAtBkQPcL0sAoed2hpkhYZpuH0D_z40FtlMTlwo3ULD_s130_assertion evidence source_evidence_literature NP424776.RAtBkQPcL0sAoed2hpkhYZpuH0D_z40FtlMTlwo3ULD_s130_provenance.
- NP424776.RAtBkQPcL0sAoed2hpkhYZpuH0D_z40FtlMTlwo3ULD_s130_assertion SIO_000772 16097850 NP424776.RAtBkQPcL0sAoed2hpkhYZpuH0D_z40FtlMTlwo3ULD_s130_provenance.
- NP424776.RAtBkQPcL0sAoed2hpkhYZpuH0D_z40FtlMTlwo3ULD_s130_assertion wasDerivedFrom befree-20140225 NP424776.RAtBkQPcL0sAoed2hpkhYZpuH0D_z40FtlMTlwo3ULD_s130_provenance.
- NP424776.RAtBkQPcL0sAoed2hpkhYZpuH0D_z40FtlMTlwo3ULD_s130_assertion wasGeneratedBy ECO_0000203 NP424776.RAtBkQPcL0sAoed2hpkhYZpuH0D_z40FtlMTlwo3ULD_s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP424776.RAtBkQPcL0sAoed2hpkhYZpuH0D_z40FtlMTlwo3ULD_s130_provenance.