Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1189293.RAFC0sV4xbvpwnd74vitZB1RfVNdb2SsBqq10VUbjti-A130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1189293.RAFC0sV4xbvpwnd74vitZB1RfVNdb2SsBqq10VUbjti-A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1189293.RAFC0sV4xbvpwnd74vitZB1RfVNdb2SsBqq10VUbjti-A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1189293.RAFC0sV4xbvpwnd74vitZB1RfVNdb2SsBqq10VUbjti-A130_provenance.
- NP1189293.RAFC0sV4xbvpwnd74vitZB1RfVNdb2SsBqq10VUbjti-A130_assertion description "[Whole-exome sequencing in an individual with severe global developmental delay and intractable epilepsy identifies a novel, de novo GRIN2A mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1189293.RAFC0sV4xbvpwnd74vitZB1RfVNdb2SsBqq10VUbjti-A130_provenance.
- NP1189293.RAFC0sV4xbvpwnd74vitZB1RfVNdb2SsBqq10VUbjti-A130_assertion evidence source_evidence_literature NP1189293.RAFC0sV4xbvpwnd74vitZB1RfVNdb2SsBqq10VUbjti-A130_provenance.
- NP1189293.RAFC0sV4xbvpwnd74vitZB1RfVNdb2SsBqq10VUbjti-A130_assertion SIO_000772 24903190 NP1189293.RAFC0sV4xbvpwnd74vitZB1RfVNdb2SsBqq10VUbjti-A130_provenance.
- NP1189293.RAFC0sV4xbvpwnd74vitZB1RfVNdb2SsBqq10VUbjti-A130_assertion wasDerivedFrom befree-2016 NP1189293.RAFC0sV4xbvpwnd74vitZB1RfVNdb2SsBqq10VUbjti-A130_provenance.
- NP1189293.RAFC0sV4xbvpwnd74vitZB1RfVNdb2SsBqq10VUbjti-A130_assertion wasGeneratedBy ECO_0000203 NP1189293.RAFC0sV4xbvpwnd74vitZB1RfVNdb2SsBqq10VUbjti-A130_provenance.
- befree-2016 importedOn "2016-02-19" NP1189293.RAFC0sV4xbvpwnd74vitZB1RfVNdb2SsBqq10VUbjti-A130_provenance.