Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1021098.RAYLkKt4ERgnzNIPlFqEK884dSRBIQk-hw6CjHtCHNQjc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1021098.RAYLkKt4ERgnzNIPlFqEK884dSRBIQk-hw6CjHtCHNQjc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1021098.RAYLkKt4ERgnzNIPlFqEK884dSRBIQk-hw6CjHtCHNQjc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1021098.RAYLkKt4ERgnzNIPlFqEK884dSRBIQk-hw6CjHtCHNQjc130_provenance.
- NP1021098.RAYLkKt4ERgnzNIPlFqEK884dSRBIQk-hw6CjHtCHNQjc130_assertion description "[Nerve excitability studies were performed on eight adults with KCNQ2 mutations and a history of benign familial neonatal epilepsy, now in remission.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1021098.RAYLkKt4ERgnzNIPlFqEK884dSRBIQk-hw6CjHtCHNQjc130_provenance.
- NP1021098.RAYLkKt4ERgnzNIPlFqEK884dSRBIQk-hw6CjHtCHNQjc130_assertion evidence source_evidence_literature NP1021098.RAYLkKt4ERgnzNIPlFqEK884dSRBIQk-hw6CjHtCHNQjc130_provenance.
- NP1021098.RAYLkKt4ERgnzNIPlFqEK884dSRBIQk-hw6CjHtCHNQjc130_assertion SIO_000772 23065794 NP1021098.RAYLkKt4ERgnzNIPlFqEK884dSRBIQk-hw6CjHtCHNQjc130_provenance.
- NP1021098.RAYLkKt4ERgnzNIPlFqEK884dSRBIQk-hw6CjHtCHNQjc130_assertion wasDerivedFrom befree-2016 NP1021098.RAYLkKt4ERgnzNIPlFqEK884dSRBIQk-hw6CjHtCHNQjc130_provenance.
- NP1021098.RAYLkKt4ERgnzNIPlFqEK884dSRBIQk-hw6CjHtCHNQjc130_assertion wasGeneratedBy ECO_0000203 NP1021098.RAYLkKt4ERgnzNIPlFqEK884dSRBIQk-hw6CjHtCHNQjc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1021098.RAYLkKt4ERgnzNIPlFqEK884dSRBIQk-hw6CjHtCHNQjc130_provenance.