Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978181.RA-4BzFB5wEyJMHI7FOvOvgMA-CS_7BQf3oGj5O3LOkrY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP978181.RA-4BzFB5wEyJMHI7FOvOvgMA-CS_7BQf3oGj5O3LOkrY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978181.RA-4BzFB5wEyJMHI7FOvOvgMA-CS_7BQf3oGj5O3LOkrY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978181.RA-4BzFB5wEyJMHI7FOvOvgMA-CS_7BQf3oGj5O3LOkrY130_provenance.
- NP978181.RA-4BzFB5wEyJMHI7FOvOvgMA-CS_7BQf3oGj5O3LOkrY130_assertion description "[To investigate the pathogenic role of ARX in refractory epilepsy of early onset even in females, we have screened the ARX sequence in a population of 50 female subjects affected with unexplained epileptic encephalopathy with onset in the first year of life.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978181.RA-4BzFB5wEyJMHI7FOvOvgMA-CS_7BQf3oGj5O3LOkrY130_provenance.
- NP978181.RA-4BzFB5wEyJMHI7FOvOvgMA-CS_7BQf3oGj5O3LOkrY130_assertion evidence source_evidence_literature NP978181.RA-4BzFB5wEyJMHI7FOvOvgMA-CS_7BQf3oGj5O3LOkrY130_provenance.
- NP978181.RA-4BzFB5wEyJMHI7FOvOvgMA-CS_7BQf3oGj5O3LOkrY130_assertion SIO_000772 23039062 NP978181.RA-4BzFB5wEyJMHI7FOvOvgMA-CS_7BQf3oGj5O3LOkrY130_provenance.
- NP978181.RA-4BzFB5wEyJMHI7FOvOvgMA-CS_7BQf3oGj5O3LOkrY130_assertion wasDerivedFrom befree-20150227 NP978181.RA-4BzFB5wEyJMHI7FOvOvgMA-CS_7BQf3oGj5O3LOkrY130_provenance.
- NP978181.RA-4BzFB5wEyJMHI7FOvOvgMA-CS_7BQf3oGj5O3LOkrY130_assertion wasGeneratedBy ECO_0000203 NP978181.RA-4BzFB5wEyJMHI7FOvOvgMA-CS_7BQf3oGj5O3LOkrY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978181.RA-4BzFB5wEyJMHI7FOvOvgMA-CS_7BQf3oGj5O3LOkrY130_provenance.