Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP628487.RAflK8SU2DxqooN5kywKyQUnpU1At3jQrXeS7JON00SAE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP628487.RAflK8SU2DxqooN5kywKyQUnpU1At3jQrXeS7JON00SAE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP628487.RAflK8SU2DxqooN5kywKyQUnpU1At3jQrXeS7JON00SAE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP628487.RAflK8SU2DxqooN5kywKyQUnpU1At3jQrXeS7JON00SAE130_provenance.
- NP628487.RAflK8SU2DxqooN5kywKyQUnpU1At3jQrXeS7JON00SAE130_assertion description "[The identification of GRIN2A as a major gene for these epileptic encephalopathies provides crucial insights into the underlying pathophysiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP628487.RAflK8SU2DxqooN5kywKyQUnpU1At3jQrXeS7JON00SAE130_provenance.
- NP628487.RAflK8SU2DxqooN5kywKyQUnpU1At3jQrXeS7JON00SAE130_assertion evidence source_evidence_literature NP628487.RAflK8SU2DxqooN5kywKyQUnpU1At3jQrXeS7JON00SAE130_provenance.
- NP628487.RAflK8SU2DxqooN5kywKyQUnpU1At3jQrXeS7JON00SAE130_assertion SIO_000772 23933820 NP628487.RAflK8SU2DxqooN5kywKyQUnpU1At3jQrXeS7JON00SAE130_provenance.
- NP628487.RAflK8SU2DxqooN5kywKyQUnpU1At3jQrXeS7JON00SAE130_assertion wasDerivedFrom befree-20140225 NP628487.RAflK8SU2DxqooN5kywKyQUnpU1At3jQrXeS7JON00SAE130_provenance.
- NP628487.RAflK8SU2DxqooN5kywKyQUnpU1At3jQrXeS7JON00SAE130_assertion wasGeneratedBy ECO_0000203 NP628487.RAflK8SU2DxqooN5kywKyQUnpU1At3jQrXeS7JON00SAE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP628487.RAflK8SU2DxqooN5kywKyQUnpU1At3jQrXeS7JON00SAE130_provenance.