Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP987418.RAh5p9TDXnbfJC6Rp5MaR0VrYdMEiP0D5tWuiBZFRzL74130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP987418.RAh5p9TDXnbfJC6Rp5MaR0VrYdMEiP0D5tWuiBZFRzL74130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP987418.RAh5p9TDXnbfJC6Rp5MaR0VrYdMEiP0D5tWuiBZFRzL74130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP987418.RAh5p9TDXnbfJC6Rp5MaR0VrYdMEiP0D5tWuiBZFRzL74130_provenance.
- NP987418.RAh5p9TDXnbfJC6Rp5MaR0VrYdMEiP0D5tWuiBZFRzL74130_assertion description "[Partial deletion of GLRB and GRIA2 in a patient with intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP987418.RAh5p9TDXnbfJC6Rp5MaR0VrYdMEiP0D5tWuiBZFRzL74130_provenance.
- NP987418.RAh5p9TDXnbfJC6Rp5MaR0VrYdMEiP0D5tWuiBZFRzL74130_assertion evidence source_evidence_literature NP987418.RAh5p9TDXnbfJC6Rp5MaR0VrYdMEiP0D5tWuiBZFRzL74130_provenance.
- NP987418.RAh5p9TDXnbfJC6Rp5MaR0VrYdMEiP0D5tWuiBZFRzL74130_assertion SIO_000772 22669415 NP987418.RAh5p9TDXnbfJC6Rp5MaR0VrYdMEiP0D5tWuiBZFRzL74130_provenance.
- NP987418.RAh5p9TDXnbfJC6Rp5MaR0VrYdMEiP0D5tWuiBZFRzL74130_assertion wasDerivedFrom befree-2016 NP987418.RAh5p9TDXnbfJC6Rp5MaR0VrYdMEiP0D5tWuiBZFRzL74130_provenance.
- NP987418.RAh5p9TDXnbfJC6Rp5MaR0VrYdMEiP0D5tWuiBZFRzL74130_assertion wasGeneratedBy ECO_0000203 NP987418.RAh5p9TDXnbfJC6Rp5MaR0VrYdMEiP0D5tWuiBZFRzL74130_provenance.
- befree-2016 importedOn "2016-02-19" NP987418.RAh5p9TDXnbfJC6Rp5MaR0VrYdMEiP0D5tWuiBZFRzL74130_provenance.