Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP729308.RA8OKGb8LcV1N65D-5LrlPqKQldnzziQUJwjXb513rpPM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP729308.RA8OKGb8LcV1N65D-5LrlPqKQldnzziQUJwjXb513rpPM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP729308.RA8OKGb8LcV1N65D-5LrlPqKQldnzziQUJwjXb513rpPM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP729308.RA8OKGb8LcV1N65D-5LrlPqKQldnzziQUJwjXb513rpPM130_provenance.
- NP729308.RA8OKGb8LcV1N65D-5LrlPqKQldnzziQUJwjXb513rpPM130_assertion description "[GRIN2A mutations cause epilepsy-aphasia spectrum disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP729308.RA8OKGb8LcV1N65D-5LrlPqKQldnzziQUJwjXb513rpPM130_provenance.
- NP729308.RA8OKGb8LcV1N65D-5LrlPqKQldnzziQUJwjXb513rpPM130_assertion evidence source_evidence_literature NP729308.RA8OKGb8LcV1N65D-5LrlPqKQldnzziQUJwjXb513rpPM130_provenance.
- NP729308.RA8OKGb8LcV1N65D-5LrlPqKQldnzziQUJwjXb513rpPM130_assertion SIO_000772 23933818 NP729308.RA8OKGb8LcV1N65D-5LrlPqKQldnzziQUJwjXb513rpPM130_provenance.
- NP729308.RA8OKGb8LcV1N65D-5LrlPqKQldnzziQUJwjXb513rpPM130_assertion wasDerivedFrom befree-20140225 NP729308.RA8OKGb8LcV1N65D-5LrlPqKQldnzziQUJwjXb513rpPM130_provenance.
- NP729308.RA8OKGb8LcV1N65D-5LrlPqKQldnzziQUJwjXb513rpPM130_assertion wasGeneratedBy ECO_0000203 NP729308.RA8OKGb8LcV1N65D-5LrlPqKQldnzziQUJwjXb513rpPM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP729308.RA8OKGb8LcV1N65D-5LrlPqKQldnzziQUJwjXb513rpPM130_provenance.