Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP313106.RArdSf1jnvL6FKGEiTbXe1JYaN8V6ljMk2E6ZiuDQxpcQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP313106.RArdSf1jnvL6FKGEiTbXe1JYaN8V6ljMk2E6ZiuDQxpcQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP313106.RArdSf1jnvL6FKGEiTbXe1JYaN8V6ljMk2E6ZiuDQxpcQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP313106.RArdSf1jnvL6FKGEiTbXe1JYaN8V6ljMk2E6ZiuDQxpcQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP313106.RArdSf1jnvL6FKGEiTbXe1JYaN8V6ljMk2E6ZiuDQxpcQ130_provenance.
- NP313106.RArdSf1jnvL6FKGEiTbXe1JYaN8V6ljMk2E6ZiuDQxpcQ130_assertion wasGeneratedBy ECO_0000203 NP313106.RArdSf1jnvL6FKGEiTbXe1JYaN8V6ljMk2E6ZiuDQxpcQ130_provenance.
- NP313106.RArdSf1jnvL6FKGEiTbXe1JYaN8V6ljMk2E6ZiuDQxpcQ130_assertion wasDerivedFrom befree-2016 NP313106.RArdSf1jnvL6FKGEiTbXe1JYaN8V6ljMk2E6ZiuDQxpcQ130_provenance.
- NP313106.RArdSf1jnvL6FKGEiTbXe1JYaN8V6ljMk2E6ZiuDQxpcQ130_assertion SIO_000772 11285244 NP313106.RArdSf1jnvL6FKGEiTbXe1JYaN8V6ljMk2E6ZiuDQxpcQ130_provenance.
- NP313106.RArdSf1jnvL6FKGEiTbXe1JYaN8V6ljMk2E6ZiuDQxpcQ130_assertion evidence source_evidence_literature NP313106.RArdSf1jnvL6FKGEiTbXe1JYaN8V6ljMk2E6ZiuDQxpcQ130_provenance.
- NP313106.RArdSf1jnvL6FKGEiTbXe1JYaN8V6ljMk2E6ZiuDQxpcQ130_assertion description "[The central nervous system malformations seen in patients with ZIC2 mutations ranged from alobar HPE (most common) to middle interhemispheric fusion defect (one case).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP313106.RArdSf1jnvL6FKGEiTbXe1JYaN8V6ljMk2E6ZiuDQxpcQ130_provenance.