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- source_evidence_literature type ECO_0000212 NP783605.RAMunJ62Z502vcBiif6r03gp1tBGD9Fd4uej_YfX7NoUs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP783605.RAMunJ62Z502vcBiif6r03gp1tBGD9Fd4uej_YfX7NoUs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP783605.RAMunJ62Z502vcBiif6r03gp1tBGD9Fd4uej_YfX7NoUs130_provenance.
- NP783605.RAMunJ62Z502vcBiif6r03gp1tBGD9Fd4uej_YfX7NoUs130_assertion description "[Results from our study indicate the involvement of SYN2 gene polymorphism in conferring risk to epilepsy; however, the genetic variant does not seem to modulate drug-response in epilepsy pharmacotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783605.RAMunJ62Z502vcBiif6r03gp1tBGD9Fd4uej_YfX7NoUs130_provenance.
- NP783605.RAMunJ62Z502vcBiif6r03gp1tBGD9Fd4uej_YfX7NoUs130_assertion evidence source_evidence_literature NP783605.RAMunJ62Z502vcBiif6r03gp1tBGD9Fd4uej_YfX7NoUs130_provenance.
- NP783605.RAMunJ62Z502vcBiif6r03gp1tBGD9Fd4uej_YfX7NoUs130_assertion SIO_000772 20034013 NP783605.RAMunJ62Z502vcBiif6r03gp1tBGD9Fd4uej_YfX7NoUs130_provenance.
- NP783605.RAMunJ62Z502vcBiif6r03gp1tBGD9Fd4uej_YfX7NoUs130_assertion wasDerivedFrom befree-2016 NP783605.RAMunJ62Z502vcBiif6r03gp1tBGD9Fd4uej_YfX7NoUs130_provenance.
- NP783605.RAMunJ62Z502vcBiif6r03gp1tBGD9Fd4uej_YfX7NoUs130_assertion wasGeneratedBy ECO_0000203 NP783605.RAMunJ62Z502vcBiif6r03gp1tBGD9Fd4uej_YfX7NoUs130_provenance.
- befree-2016 importedOn "2016-02-19" NP783605.RAMunJ62Z502vcBiif6r03gp1tBGD9Fd4uej_YfX7NoUs130_provenance.