Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP534156.RA7OvpmA55FLnE2vrQIQn3P2VYBoeULR_n5M6JhEB0xUA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP534156.RA7OvpmA55FLnE2vrQIQn3P2VYBoeULR_n5M6JhEB0xUA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP534156.RA7OvpmA55FLnE2vrQIQn3P2VYBoeULR_n5M6JhEB0xUA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP534156.RA7OvpmA55FLnE2vrQIQn3P2VYBoeULR_n5M6JhEB0xUA130_provenance.
- NP534156.RA7OvpmA55FLnE2vrQIQn3P2VYBoeULR_n5M6JhEB0xUA130_assertion description "[We selected rs3773364 A>G polymorphism in SYN2 gene and analyzed its distribution in north Indian patients with epilepsy and control subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP534156.RA7OvpmA55FLnE2vrQIQn3P2VYBoeULR_n5M6JhEB0xUA130_provenance.
- NP534156.RA7OvpmA55FLnE2vrQIQn3P2VYBoeULR_n5M6JhEB0xUA130_assertion evidence source_evidence_literature NP534156.RA7OvpmA55FLnE2vrQIQn3P2VYBoeULR_n5M6JhEB0xUA130_provenance.
- NP534156.RA7OvpmA55FLnE2vrQIQn3P2VYBoeULR_n5M6JhEB0xUA130_assertion SIO_000772 20034013 NP534156.RA7OvpmA55FLnE2vrQIQn3P2VYBoeULR_n5M6JhEB0xUA130_provenance.
- NP534156.RA7OvpmA55FLnE2vrQIQn3P2VYBoeULR_n5M6JhEB0xUA130_assertion wasDerivedFrom befree-20140225 NP534156.RA7OvpmA55FLnE2vrQIQn3P2VYBoeULR_n5M6JhEB0xUA130_provenance.
- NP534156.RA7OvpmA55FLnE2vrQIQn3P2VYBoeULR_n5M6JhEB0xUA130_assertion wasGeneratedBy ECO_0000203 NP534156.RA7OvpmA55FLnE2vrQIQn3P2VYBoeULR_n5M6JhEB0xUA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP534156.RA7OvpmA55FLnE2vrQIQn3P2VYBoeULR_n5M6JhEB0xUA130_provenance.