Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1219854.RAnjwNM6eofy-9bj3SI24Aw2vx2rGVWbpuSmfxil-APIQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1219854.RAnjwNM6eofy-9bj3SI24Aw2vx2rGVWbpuSmfxil-APIQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1219854.RAnjwNM6eofy-9bj3SI24Aw2vx2rGVWbpuSmfxil-APIQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1219854.RAnjwNM6eofy-9bj3SI24Aw2vx2rGVWbpuSmfxil-APIQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1219854.RAnjwNM6eofy-9bj3SI24Aw2vx2rGVWbpuSmfxil-APIQ130_provenance.
- NP1219854.RAnjwNM6eofy-9bj3SI24Aw2vx2rGVWbpuSmfxil-APIQ130_assertion wasGeneratedBy ECO_0000203 NP1219854.RAnjwNM6eofy-9bj3SI24Aw2vx2rGVWbpuSmfxil-APIQ130_provenance.
- NP1219854.RAnjwNM6eofy-9bj3SI24Aw2vx2rGVWbpuSmfxil-APIQ130_assertion wasDerivedFrom befree-2016 NP1219854.RAnjwNM6eofy-9bj3SI24Aw2vx2rGVWbpuSmfxil-APIQ130_provenance.
- NP1219854.RAnjwNM6eofy-9bj3SI24Aw2vx2rGVWbpuSmfxil-APIQ130_assertion SIO_000772 25218114 NP1219854.RAnjwNM6eofy-9bj3SI24Aw2vx2rGVWbpuSmfxil-APIQ130_provenance.
- NP1219854.RAnjwNM6eofy-9bj3SI24Aw2vx2rGVWbpuSmfxil-APIQ130_assertion evidence source_evidence_literature NP1219854.RAnjwNM6eofy-9bj3SI24Aw2vx2rGVWbpuSmfxil-APIQ130_provenance.
- NP1219854.RAnjwNM6eofy-9bj3SI24Aw2vx2rGVWbpuSmfxil-APIQ130_assertion description "[The present findings confirm that PCDH19 is a major causative gene for infantile onset familial or sporadic epilepsy in female patients with or without mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1219854.RAnjwNM6eofy-9bj3SI24Aw2vx2rGVWbpuSmfxil-APIQ130_provenance.