Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP259124.RACCauRj_EB9PrjsVsAQWbRzZWb5UJdnc7tcITY0TjNM4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP259124.RACCauRj_EB9PrjsVsAQWbRzZWb5UJdnc7tcITY0TjNM4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP259124.RACCauRj_EB9PrjsVsAQWbRzZWb5UJdnc7tcITY0TjNM4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP259124.RACCauRj_EB9PrjsVsAQWbRzZWb5UJdnc7tcITY0TjNM4130_provenance.
- befree-2016 importedOn "2016-02-19" NP259124.RACCauRj_EB9PrjsVsAQWbRzZWb5UJdnc7tcITY0TjNM4130_provenance.
- NP259124.RACCauRj_EB9PrjsVsAQWbRzZWb5UJdnc7tcITY0TjNM4130_assertion wasGeneratedBy ECO_0000203 NP259124.RACCauRj_EB9PrjsVsAQWbRzZWb5UJdnc7tcITY0TjNM4130_provenance.
- NP259124.RACCauRj_EB9PrjsVsAQWbRzZWb5UJdnc7tcITY0TjNM4130_assertion wasDerivedFrom befree-2016 NP259124.RACCauRj_EB9PrjsVsAQWbRzZWb5UJdnc7tcITY0TjNM4130_provenance.
- NP259124.RACCauRj_EB9PrjsVsAQWbRzZWb5UJdnc7tcITY0TjNM4130_assertion SIO_000772 10430413 NP259124.RACCauRj_EB9PrjsVsAQWbRzZWb5UJdnc7tcITY0TjNM4130_provenance.
- NP259124.RACCauRj_EB9PrjsVsAQWbRzZWb5UJdnc7tcITY0TjNM4130_assertion evidence source_evidence_literature NP259124.RACCauRj_EB9PrjsVsAQWbRzZWb5UJdnc7tcITY0TjNM4130_provenance.
- NP259124.RACCauRj_EB9PrjsVsAQWbRzZWb5UJdnc7tcITY0TjNM4130_assertion description "[We found consistent differences in the gyral patterns, with the malformation more severe posteriorly in individuals with LIS1 mutations and more severe anteriorly in individuals with XLIS mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP259124.RACCauRj_EB9PrjsVsAQWbRzZWb5UJdnc7tcITY0TjNM4130_provenance.