Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP277229.RACpFc_jVcQ4k3u48BQAyvlQQvuDGU_NHk_CgPoi034x4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP277229.RACpFc_jVcQ4k3u48BQAyvlQQvuDGU_NHk_CgPoi034x4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP277229.RACpFc_jVcQ4k3u48BQAyvlQQvuDGU_NHk_CgPoi034x4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP277229.RACpFc_jVcQ4k3u48BQAyvlQQvuDGU_NHk_CgPoi034x4130_provenance.
- NP277229.RACpFc_jVcQ4k3u48BQAyvlQQvuDGU_NHk_CgPoi034x4130_assertion description "[Previous studies implicate CACNA1C (L-type Ca(V)1.2) calcium channel mutations in a disorder associated with autism (Timothy syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP277229.RACpFc_jVcQ4k3u48BQAyvlQQvuDGU_NHk_CgPoi034x4130_provenance.
- NP277229.RACpFc_jVcQ4k3u48BQAyvlQQvuDGU_NHk_CgPoi034x4130_assertion evidence source_evidence_literature NP277229.RACpFc_jVcQ4k3u48BQAyvlQQvuDGU_NHk_CgPoi034x4130_provenance.
- NP277229.RACpFc_jVcQ4k3u48BQAyvlQQvuDGU_NHk_CgPoi034x4130_assertion SIO_000772 16754686 NP277229.RACpFc_jVcQ4k3u48BQAyvlQQvuDGU_NHk_CgPoi034x4130_provenance.
- NP277229.RACpFc_jVcQ4k3u48BQAyvlQQvuDGU_NHk_CgPoi034x4130_assertion wasDerivedFrom befree-20150227 NP277229.RACpFc_jVcQ4k3u48BQAyvlQQvuDGU_NHk_CgPoi034x4130_provenance.
- NP277229.RACpFc_jVcQ4k3u48BQAyvlQQvuDGU_NHk_CgPoi034x4130_assertion wasGeneratedBy ECO_0000203 NP277229.RACpFc_jVcQ4k3u48BQAyvlQQvuDGU_NHk_CgPoi034x4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP277229.RACpFc_jVcQ4k3u48BQAyvlQQvuDGU_NHk_CgPoi034x4130_provenance.