Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP557117.RAlGIrINR0arIaC8Zuf3MS0wvPLT3eI87Dx0Y0rsu9HFg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP557117.RAlGIrINR0arIaC8Zuf3MS0wvPLT3eI87Dx0Y0rsu9HFg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP557117.RAlGIrINR0arIaC8Zuf3MS0wvPLT3eI87Dx0Y0rsu9HFg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP557117.RAlGIrINR0arIaC8Zuf3MS0wvPLT3eI87Dx0Y0rsu9HFg130_provenance.
- NP557117.RAlGIrINR0arIaC8Zuf3MS0wvPLT3eI87Dx0Y0rsu9HFg130_assertion description "[Lissencephaly caused by LIS1 or DCX mutation frequently results in West syndrome, while lissencephaly due to ARX mutation is associated with the most severe form of epilepsy but never results in West syndrome nor infantile spasms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557117.RAlGIrINR0arIaC8Zuf3MS0wvPLT3eI87Dx0Y0rsu9HFg130_provenance.
- NP557117.RAlGIrINR0arIaC8Zuf3MS0wvPLT3eI87Dx0Y0rsu9HFg130_assertion evidence source_evidence_literature NP557117.RAlGIrINR0arIaC8Zuf3MS0wvPLT3eI87Dx0Y0rsu9HFg130_provenance.
- NP557117.RAlGIrINR0arIaC8Zuf3MS0wvPLT3eI87Dx0Y0rsu9HFg130_assertion SIO_000772 16806828 NP557117.RAlGIrINR0arIaC8Zuf3MS0wvPLT3eI87Dx0Y0rsu9HFg130_provenance.
- NP557117.RAlGIrINR0arIaC8Zuf3MS0wvPLT3eI87Dx0Y0rsu9HFg130_assertion wasDerivedFrom befree-2016 NP557117.RAlGIrINR0arIaC8Zuf3MS0wvPLT3eI87Dx0Y0rsu9HFg130_provenance.
- NP557117.RAlGIrINR0arIaC8Zuf3MS0wvPLT3eI87Dx0Y0rsu9HFg130_assertion wasGeneratedBy ECO_0000203 NP557117.RAlGIrINR0arIaC8Zuf3MS0wvPLT3eI87Dx0Y0rsu9HFg130_provenance.
- befree-2016 importedOn "2016-02-19" NP557117.RAlGIrINR0arIaC8Zuf3MS0wvPLT3eI87Dx0Y0rsu9HFg130_provenance.