Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP674910.RAW_Nv9JbQUPLRdDSK9vHR_-AJiMP3Bl7nqO2hVcf6bk0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP674910.RAW_Nv9JbQUPLRdDSK9vHR_-AJiMP3Bl7nqO2hVcf6bk0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP674910.RAW_Nv9JbQUPLRdDSK9vHR_-AJiMP3Bl7nqO2hVcf6bk0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP674910.RAW_Nv9JbQUPLRdDSK9vHR_-AJiMP3Bl7nqO2hVcf6bk0130_provenance.
- NP674910.RAW_Nv9JbQUPLRdDSK9vHR_-AJiMP3Bl7nqO2hVcf6bk0130_assertion description "[The severe mental retardation and speech deficits associated with 22q13 terminal deletions have been attributed in large part to haploinsufficiency of SHANK3, which maps to all 22q13 terminal deletions, although more proximal genes are assumed to have minor effects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674910.RAW_Nv9JbQUPLRdDSK9vHR_-AJiMP3Bl7nqO2hVcf6bk0130_provenance.
- NP674910.RAW_Nv9JbQUPLRdDSK9vHR_-AJiMP3Bl7nqO2hVcf6bk0130_assertion evidence source_evidence_literature NP674910.RAW_Nv9JbQUPLRdDSK9vHR_-AJiMP3Bl7nqO2hVcf6bk0130_provenance.
- NP674910.RAW_Nv9JbQUPLRdDSK9vHR_-AJiMP3Bl7nqO2hVcf6bk0130_assertion SIO_000772 18523453 NP674910.RAW_Nv9JbQUPLRdDSK9vHR_-AJiMP3Bl7nqO2hVcf6bk0130_provenance.
- NP674910.RAW_Nv9JbQUPLRdDSK9vHR_-AJiMP3Bl7nqO2hVcf6bk0130_assertion wasDerivedFrom befree-2016 NP674910.RAW_Nv9JbQUPLRdDSK9vHR_-AJiMP3Bl7nqO2hVcf6bk0130_provenance.
- NP674910.RAW_Nv9JbQUPLRdDSK9vHR_-AJiMP3Bl7nqO2hVcf6bk0130_assertion wasGeneratedBy ECO_0000203 NP674910.RAW_Nv9JbQUPLRdDSK9vHR_-AJiMP3Bl7nqO2hVcf6bk0130_provenance.
- befree-2016 importedOn "2016-02-19" NP674910.RAW_Nv9JbQUPLRdDSK9vHR_-AJiMP3Bl7nqO2hVcf6bk0130_provenance.