Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP129196.RANhiAH7_pOK9FmOhz3N5qF1XQb3kQPicDSgP-Ue0XobI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP129196.RANhiAH7_pOK9FmOhz3N5qF1XQb3kQPicDSgP-Ue0XobI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP129196.RANhiAH7_pOK9FmOhz3N5qF1XQb3kQPicDSgP-Ue0XobI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP129196.RANhiAH7_pOK9FmOhz3N5qF1XQb3kQPicDSgP-Ue0XobI130_provenance.
- NP129196.RANhiAH7_pOK9FmOhz3N5qF1XQb3kQPicDSgP-Ue0XobI130_assertion description "[A CACNB4 mutation shows that altered Ca(v)2.1 function may be a genetic modifier of severe myoclonic epilepsy in infancy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP129196.RANhiAH7_pOK9FmOhz3N5qF1XQb3kQPicDSgP-Ue0XobI130_provenance.
- NP129196.RANhiAH7_pOK9FmOhz3N5qF1XQb3kQPicDSgP-Ue0XobI130_assertion evidence source_evidence_literature NP129196.RANhiAH7_pOK9FmOhz3N5qF1XQb3kQPicDSgP-Ue0XobI130_provenance.
- NP129196.RANhiAH7_pOK9FmOhz3N5qF1XQb3kQPicDSgP-Ue0XobI130_assertion SIO_000772 18755274 NP129196.RANhiAH7_pOK9FmOhz3N5qF1XQb3kQPicDSgP-Ue0XobI130_provenance.
- NP129196.RANhiAH7_pOK9FmOhz3N5qF1XQb3kQPicDSgP-Ue0XobI130_assertion wasDerivedFrom gad-20150221 NP129196.RANhiAH7_pOK9FmOhz3N5qF1XQb3kQPicDSgP-Ue0XobI130_provenance.
- NP129196.RANhiAH7_pOK9FmOhz3N5qF1XQb3kQPicDSgP-Ue0XobI130_assertion wasGeneratedBy ECO_0000203 NP129196.RANhiAH7_pOK9FmOhz3N5qF1XQb3kQPicDSgP-Ue0XobI130_provenance.
- gad-20150221 importedOn "2015-02-21" NP129196.RANhiAH7_pOK9FmOhz3N5qF1XQb3kQPicDSgP-Ue0XobI130_provenance.