Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP253369.RAzMUAv_EuqwqlfiQsLCYuWOGfH1vGaQ_rHPfvlLz4pHs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP253369.RAzMUAv_EuqwqlfiQsLCYuWOGfH1vGaQ_rHPfvlLz4pHs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP253369.RAzMUAv_EuqwqlfiQsLCYuWOGfH1vGaQ_rHPfvlLz4pHs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP253369.RAzMUAv_EuqwqlfiQsLCYuWOGfH1vGaQ_rHPfvlLz4pHs130_provenance.
- NP253369.RAzMUAv_EuqwqlfiQsLCYuWOGfH1vGaQ_rHPfvlLz4pHs130_assertion description "[Together, these results support a model where the DIA1 and DIA1R gene products regulate molecular traffic through the cellular secretory pathway or affect the function of secreted factors, and functional deficits cause disorders with ASD-like symptoms and/or mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP253369.RAzMUAv_EuqwqlfiQsLCYuWOGfH1vGaQ_rHPfvlLz4pHs130_provenance.
- NP253369.RAzMUAv_EuqwqlfiQsLCYuWOGfH1vGaQ_rHPfvlLz4pHs130_assertion evidence source_evidence_literature NP253369.RAzMUAv_EuqwqlfiQsLCYuWOGfH1vGaQ_rHPfvlLz4pHs130_provenance.
- NP253369.RAzMUAv_EuqwqlfiQsLCYuWOGfH1vGaQ_rHPfvlLz4pHs130_assertion SIO_000772 21264219 NP253369.RAzMUAv_EuqwqlfiQsLCYuWOGfH1vGaQ_rHPfvlLz4pHs130_provenance.
- NP253369.RAzMUAv_EuqwqlfiQsLCYuWOGfH1vGaQ_rHPfvlLz4pHs130_assertion wasDerivedFrom befree-20150227 NP253369.RAzMUAv_EuqwqlfiQsLCYuWOGfH1vGaQ_rHPfvlLz4pHs130_provenance.
- NP253369.RAzMUAv_EuqwqlfiQsLCYuWOGfH1vGaQ_rHPfvlLz4pHs130_assertion wasGeneratedBy ECO_0000203 NP253369.RAzMUAv_EuqwqlfiQsLCYuWOGfH1vGaQ_rHPfvlLz4pHs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP253369.RAzMUAv_EuqwqlfiQsLCYuWOGfH1vGaQ_rHPfvlLz4pHs130_provenance.