Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP654883.RAQ4Tlj66cYflnFzV9CQwv-GkzudMLpeoYylXmfaZ2PXg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP654883.RAQ4Tlj66cYflnFzV9CQwv-GkzudMLpeoYylXmfaZ2PXg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP654883.RAQ4Tlj66cYflnFzV9CQwv-GkzudMLpeoYylXmfaZ2PXg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP654883.RAQ4Tlj66cYflnFzV9CQwv-GkzudMLpeoYylXmfaZ2PXg130_provenance.
- NP654883.RAQ4Tlj66cYflnFzV9CQwv-GkzudMLpeoYylXmfaZ2PXg130_assertion description "[It may be worthwhile to screen patients with a combination of epilepsy and migraine and a positive family history of either migraine or epilepsy for mutations in the ATP1A2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP654883.RAQ4Tlj66cYflnFzV9CQwv-GkzudMLpeoYylXmfaZ2PXg130_provenance.
- NP654883.RAQ4Tlj66cYflnFzV9CQwv-GkzudMLpeoYylXmfaZ2PXg130_assertion evidence source_evidence_literature NP654883.RAQ4Tlj66cYflnFzV9CQwv-GkzudMLpeoYylXmfaZ2PXg130_provenance.
- NP654883.RAQ4Tlj66cYflnFzV9CQwv-GkzudMLpeoYylXmfaZ2PXg130_assertion SIO_000772 18028407 NP654883.RAQ4Tlj66cYflnFzV9CQwv-GkzudMLpeoYylXmfaZ2PXg130_provenance.
- NP654883.RAQ4Tlj66cYflnFzV9CQwv-GkzudMLpeoYylXmfaZ2PXg130_assertion wasDerivedFrom befree-20140225 NP654883.RAQ4Tlj66cYflnFzV9CQwv-GkzudMLpeoYylXmfaZ2PXg130_provenance.
- NP654883.RAQ4Tlj66cYflnFzV9CQwv-GkzudMLpeoYylXmfaZ2PXg130_assertion wasGeneratedBy ECO_0000203 NP654883.RAQ4Tlj66cYflnFzV9CQwv-GkzudMLpeoYylXmfaZ2PXg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP654883.RAQ4Tlj66cYflnFzV9CQwv-GkzudMLpeoYylXmfaZ2PXg130_provenance.