Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1219854.RAnjwNM6eofy-9bj3SI24Aw2vx2rGVWbpuSmfxil-APIQ130_assertion> ?p ?o ?g. }
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- NP1219854.RAnjwNM6eofy-9bj3SI24Aw2vx2rGVWbpuSmfxil-APIQ130_assertion type Assertion NP1219854.RAnjwNM6eofy-9bj3SI24Aw2vx2rGVWbpuSmfxil-APIQ130_head.
- 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.