Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP990684.RAvFTrVM5NAU0frMCBG_rUdqJaEV_JNkt_-QP_r_t_CG4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP990684.RAvFTrVM5NAU0frMCBG_rUdqJaEV_JNkt_-QP_r_t_CG4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP990684.RAvFTrVM5NAU0frMCBG_rUdqJaEV_JNkt_-QP_r_t_CG4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP990684.RAvFTrVM5NAU0frMCBG_rUdqJaEV_JNkt_-QP_r_t_CG4130_provenance.
- NP990684.RAvFTrVM5NAU0frMCBG_rUdqJaEV_JNkt_-QP_r_t_CG4130_assertion description "[Genetic variation in CACNA1C have also been associated with depression, schizophrenia, autism spectrum disorders, as well as changes in brain function and structure in control subjects who have no diagnosable psychiatric illness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP990684.RAvFTrVM5NAU0frMCBG_rUdqJaEV_JNkt_-QP_r_t_CG4130_provenance.
- NP990684.RAvFTrVM5NAU0frMCBG_rUdqJaEV_JNkt_-QP_r_t_CG4130_assertion evidence source_evidence_literature NP990684.RAvFTrVM5NAU0frMCBG_rUdqJaEV_JNkt_-QP_r_t_CG4130_provenance.
- NP990684.RAvFTrVM5NAU0frMCBG_rUdqJaEV_JNkt_-QP_r_t_CG4130_assertion SIO_000772 22705413 NP990684.RAvFTrVM5NAU0frMCBG_rUdqJaEV_JNkt_-QP_r_t_CG4130_provenance.
- NP990684.RAvFTrVM5NAU0frMCBG_rUdqJaEV_JNkt_-QP_r_t_CG4130_assertion wasDerivedFrom befree-2016 NP990684.RAvFTrVM5NAU0frMCBG_rUdqJaEV_JNkt_-QP_r_t_CG4130_provenance.
- NP990684.RAvFTrVM5NAU0frMCBG_rUdqJaEV_JNkt_-QP_r_t_CG4130_assertion wasGeneratedBy ECO_0000203 NP990684.RAvFTrVM5NAU0frMCBG_rUdqJaEV_JNkt_-QP_r_t_CG4130_provenance.
- befree-2016 importedOn "2016-02-19" NP990684.RAvFTrVM5NAU0frMCBG_rUdqJaEV_JNkt_-QP_r_t_CG4130_provenance.