Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP915272.RAqxgGWSE4aDOEHABSrCOpBBi0Btt_SKLYY1AAQR5uu-M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP915272.RAqxgGWSE4aDOEHABSrCOpBBi0Btt_SKLYY1AAQR5uu-M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP915272.RAqxgGWSE4aDOEHABSrCOpBBi0Btt_SKLYY1AAQR5uu-M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP915272.RAqxgGWSE4aDOEHABSrCOpBBi0Btt_SKLYY1AAQR5uu-M130_provenance.
- NP915272.RAqxgGWSE4aDOEHABSrCOpBBi0Btt_SKLYY1AAQR5uu-M130_assertion description "[We identified 40 de novo mutations in 27 cases affecting 40 genes, including a potentially disruptive mutation in DGCR2, a gene located in the schizophrenia-predisposing 22q11.2 microdeletion region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP915272.RAqxgGWSE4aDOEHABSrCOpBBi0Btt_SKLYY1AAQR5uu-M130_provenance.
- NP915272.RAqxgGWSE4aDOEHABSrCOpBBi0Btt_SKLYY1AAQR5uu-M130_assertion evidence source_evidence_literature NP915272.RAqxgGWSE4aDOEHABSrCOpBBi0Btt_SKLYY1AAQR5uu-M130_provenance.
- NP915272.RAqxgGWSE4aDOEHABSrCOpBBi0Btt_SKLYY1AAQR5uu-M130_assertion SIO_000772 21822266 NP915272.RAqxgGWSE4aDOEHABSrCOpBBi0Btt_SKLYY1AAQR5uu-M130_provenance.
- NP915272.RAqxgGWSE4aDOEHABSrCOpBBi0Btt_SKLYY1AAQR5uu-M130_assertion wasDerivedFrom befree-2016 NP915272.RAqxgGWSE4aDOEHABSrCOpBBi0Btt_SKLYY1AAQR5uu-M130_provenance.
- NP915272.RAqxgGWSE4aDOEHABSrCOpBBi0Btt_SKLYY1AAQR5uu-M130_assertion wasGeneratedBy ECO_0000203 NP915272.RAqxgGWSE4aDOEHABSrCOpBBi0Btt_SKLYY1AAQR5uu-M130_provenance.
- befree-2016 importedOn "2016-02-19" NP915272.RAqxgGWSE4aDOEHABSrCOpBBi0Btt_SKLYY1AAQR5uu-M130_provenance.