Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP217459.RAcTEIJr0YihZNYSOvn1066O_GVilNzrintavf8BUrIKQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP217459.RAcTEIJr0YihZNYSOvn1066O_GVilNzrintavf8BUrIKQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP217459.RAcTEIJr0YihZNYSOvn1066O_GVilNzrintavf8BUrIKQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP217459.RAcTEIJr0YihZNYSOvn1066O_GVilNzrintavf8BUrIKQ130_provenance.
- NP217459.RAcTEIJr0YihZNYSOvn1066O_GVilNzrintavf8BUrIKQ130_assertion wasGeneratedBy ECO_0000203 NP217459.RAcTEIJr0YihZNYSOvn1066O_GVilNzrintavf8BUrIKQ130_provenance.
- NP217459.RAcTEIJr0YihZNYSOvn1066O_GVilNzrintavf8BUrIKQ130_assertion wasDerivedFrom befree-20140225 NP217459.RAcTEIJr0YihZNYSOvn1066O_GVilNzrintavf8BUrIKQ130_provenance.
- NP217459.RAcTEIJr0YihZNYSOvn1066O_GVilNzrintavf8BUrIKQ130_assertion SIO_000772 11285244 NP217459.RAcTEIJr0YihZNYSOvn1066O_GVilNzrintavf8BUrIKQ130_provenance.
- NP217459.RAcTEIJr0YihZNYSOvn1066O_GVilNzrintavf8BUrIKQ130_assertion evidence source_evidence_literature NP217459.RAcTEIJr0YihZNYSOvn1066O_GVilNzrintavf8BUrIKQ130_provenance.
- NP217459.RAcTEIJr0YihZNYSOvn1066O_GVilNzrintavf8BUrIKQ130_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." NP217459.RAcTEIJr0YihZNYSOvn1066O_GVilNzrintavf8BUrIKQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP217459.RAcTEIJr0YihZNYSOvn1066O_GVilNzrintavf8BUrIKQ130_provenance.