@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP1014434.RABeLCuP-Q9iyLELUUIA9hSUnUFw0l1QsymA78e49r82M130_head { this: np:hasAssertion dgn-np:NP1014434.RABeLCuP-Q9iyLELUUIA9hSUnUFw0l1QsymA78e49r82M130_assertion; np:hasProvenance dgn-np:NP1014434.RABeLCuP-Q9iyLELUUIA9hSUnUFw0l1QsymA78e49r82M130_provenance; np:hasPublicationInfo dgn-np:NP1014434.RABeLCuP-Q9iyLELUUIA9hSUnUFw0l1QsymA78e49r82M130_publicationInfo; a np:Nanopublication . dgn-np:NP1014434.RABeLCuP-Q9iyLELUUIA9hSUnUFw0l1QsymA78e49r82M130_assertion a np:Assertion . dgn-np:NP1014434.RABeLCuP-Q9iyLELUUIA9hSUnUFw0l1QsymA78e49r82M130_provenance a np:Provenance . dgn-np:NP1014434.RABeLCuP-Q9iyLELUUIA9hSUnUFw0l1QsymA78e49r82M130_publicationInfo a np:PublicationInfo . } dgn-np:NP1014434.RABeLCuP-Q9iyLELUUIA9hSUnUFw0l1QsymA78e49r82M130_assertion { miriam-gene:100329170 a ncit:C16612 . lld:C0036341 a ncit:C7057 . dgn-gda:DGN39edce637d2abd079e88bd98714b25a0 sio:SIO_000628 miriam-gene:100329170, lld:C0036341; a sio:SIO_001121 . } dgn-np:NP1014434.RABeLCuP-Q9iyLELUUIA9hSUnUFw0l1QsymA78e49r82M130_provenance { dgn-np:NP1014434.RABeLCuP-Q9iyLELUUIA9hSUnUFw0l1QsymA78e49r82M130_assertion dcterms:description "[In an electroencephalographic (EEG) study of 27 pairs of monozygotic (MZ) twins discordant for schizophrenia, 13 pairs of MZ twins concordant for schizophrenia, 40 pairs of healthy MZ twins, and 91 healthy, unrelated subjects with repeated assessments, we investigated (a) the trait quality of brainwave patterns with respect to interindividual differences, intraindividual stability over time, and within-pair MZ concordance; (b) the EEG characteristics that enable discrimination between affected and unaffected individuals; and (c) the EEG characteristics that reflect the severity of illness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:10098386; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP1014434.RABeLCuP-Q9iyLELUUIA9hSUnUFw0l1QsymA78e49r82M130_publicationInfo { this: dcterms:created "2015-08-25T14:48:09+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }