Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP904006.RAyyfAy5OtzP5ZFBOnwdX11iC1oZm9ATSj1E-D8s-2okE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP904006.RAyyfAy5OtzP5ZFBOnwdX11iC1oZm9ATSj1E-D8s-2okE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP904006.RAyyfAy5OtzP5ZFBOnwdX11iC1oZm9ATSj1E-D8s-2okE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP904006.RAyyfAy5OtzP5ZFBOnwdX11iC1oZm9ATSj1E-D8s-2okE130_provenance.
- befree-2016 importedOn "2016-02-19" NP904006.RAyyfAy5OtzP5ZFBOnwdX11iC1oZm9ATSj1E-D8s-2okE130_provenance.
- NP904006.RAyyfAy5OtzP5ZFBOnwdX11iC1oZm9ATSj1E-D8s-2okE130_assertion wasGeneratedBy ECO_0000203 NP904006.RAyyfAy5OtzP5ZFBOnwdX11iC1oZm9ATSj1E-D8s-2okE130_provenance.
- NP904006.RAyyfAy5OtzP5ZFBOnwdX11iC1oZm9ATSj1E-D8s-2okE130_assertion wasDerivedFrom befree-2016 NP904006.RAyyfAy5OtzP5ZFBOnwdX11iC1oZm9ATSj1E-D8s-2okE130_provenance.
- NP904006.RAyyfAy5OtzP5ZFBOnwdX11iC1oZm9ATSj1E-D8s-2okE130_assertion SIO_000772 21694734 NP904006.RAyyfAy5OtzP5ZFBOnwdX11iC1oZm9ATSj1E-D8s-2okE130_provenance.
- NP904006.RAyyfAy5OtzP5ZFBOnwdX11iC1oZm9ATSj1E-D8s-2okE130_assertion evidence source_evidence_literature NP904006.RAyyfAy5OtzP5ZFBOnwdX11iC1oZm9ATSj1E-D8s-2okE130_provenance.
- NP904006.RAyyfAy5OtzP5ZFBOnwdX11iC1oZm9ATSj1E-D8s-2okE130_assertion description "[Finally, we provide evidence that ISS in deletion 1p36 may be associated with deletion of KLHL17 and expand the epilepsy phenotype in that syndrome to include early infantile epileptic encephalopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP904006.RAyyfAy5OtzP5ZFBOnwdX11iC1oZm9ATSj1E-D8s-2okE130_provenance.