Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP434487.RA-x4EMwkj_B7LMrMcR6-0-TfaG_SKqmm_ZPGBZQZH1Y8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP434487.RA-x4EMwkj_B7LMrMcR6-0-TfaG_SKqmm_ZPGBZQZH1Y8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP434487.RA-x4EMwkj_B7LMrMcR6-0-TfaG_SKqmm_ZPGBZQZH1Y8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP434487.RA-x4EMwkj_B7LMrMcR6-0-TfaG_SKqmm_ZPGBZQZH1Y8130_provenance.
- NP434487.RA-x4EMwkj_B7LMrMcR6-0-TfaG_SKqmm_ZPGBZQZH1Y8130_assertion description "[Deletions in 16p13 including GRIN2A in patients with intellectual disability, various dysmorphic features, and seizure disorders of the rolandic region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP434487.RA-x4EMwkj_B7LMrMcR6-0-TfaG_SKqmm_ZPGBZQZH1Y8130_provenance.
- NP434487.RA-x4EMwkj_B7LMrMcR6-0-TfaG_SKqmm_ZPGBZQZH1Y8130_assertion evidence source_evidence_literature NP434487.RA-x4EMwkj_B7LMrMcR6-0-TfaG_SKqmm_ZPGBZQZH1Y8130_provenance.
- NP434487.RA-x4EMwkj_B7LMrMcR6-0-TfaG_SKqmm_ZPGBZQZH1Y8130_assertion SIO_000772 20384727 NP434487.RA-x4EMwkj_B7LMrMcR6-0-TfaG_SKqmm_ZPGBZQZH1Y8130_provenance.
- NP434487.RA-x4EMwkj_B7LMrMcR6-0-TfaG_SKqmm_ZPGBZQZH1Y8130_assertion wasDerivedFrom befree-20150227 NP434487.RA-x4EMwkj_B7LMrMcR6-0-TfaG_SKqmm_ZPGBZQZH1Y8130_provenance.
- NP434487.RA-x4EMwkj_B7LMrMcR6-0-TfaG_SKqmm_ZPGBZQZH1Y8130_assertion wasGeneratedBy ECO_0000203 NP434487.RA-x4EMwkj_B7LMrMcR6-0-TfaG_SKqmm_ZPGBZQZH1Y8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP434487.RA-x4EMwkj_B7LMrMcR6-0-TfaG_SKqmm_ZPGBZQZH1Y8130_provenance.