@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:NP937614.RAAkGweUgdQvnoU6ffcYf8CYfVYSxsZW8MTld-Qm-W__o130_head { this: np:hasAssertion dgn-np:NP937614.RAAkGweUgdQvnoU6ffcYf8CYfVYSxsZW8MTld-Qm-W__o130_assertion; np:hasProvenance dgn-np:NP937614.RAAkGweUgdQvnoU6ffcYf8CYfVYSxsZW8MTld-Qm-W__o130_provenance; np:hasPublicationInfo dgn-np:NP937614.RAAkGweUgdQvnoU6ffcYf8CYfVYSxsZW8MTld-Qm-W__o130_publicationInfo; a np:Nanopublication . dgn-np:NP937614.RAAkGweUgdQvnoU6ffcYf8CYfVYSxsZW8MTld-Qm-W__o130_assertion a np:Assertion . dgn-np:NP937614.RAAkGweUgdQvnoU6ffcYf8CYfVYSxsZW8MTld-Qm-W__o130_provenance a np:Provenance . dgn-np:NP937614.RAAkGweUgdQvnoU6ffcYf8CYfVYSxsZW8MTld-Qm-W__o130_publicationInfo a np:PublicationInfo . } dgn-np:NP937614.RAAkGweUgdQvnoU6ffcYf8CYfVYSxsZW8MTld-Qm-W__o130_assertion { miriam-gene:414 a ncit:C16612 . lld:C0004936 a ncit:C7057 . dgn-gda:DGN157e5c0cee4e4b0b7299f12a995d47ed sio:SIO_000628 miriam-gene:414, lld:C0004936; a sio:SIO_001121 . } dgn-np:NP937614.RAAkGweUgdQvnoU6ffcYf8CYfVYSxsZW8MTld-Qm-W__o130_provenance { dgn-np:NP937614.RAAkGweUgdQvnoU6ffcYf8CYfVYSxsZW8MTld-Qm-W__o130_assertion dcterms:description "[This review addresses the particular issues that attend gene discovery in neuropsychiatric and neurodevelopmental disorders and ASDs in particular, summarizes recent findings in human genetics broadly that are driving the reevaluation of the conventional wisdom regarding the allelic architecture of common psychiatric conditions, reviews selected discoveries in ASDs and their relevance to models of pathology, highlights the conceptual and practical issues raised by the observation of a convergence of ASD genetic risks with distinct psychiatric disorders, and considers the important interplay of studies of neurobiology and genetics in clarifying and extending our understanding of social disability syndromes.]. 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:22037497; prov:wasDerivedFrom dgn-void:befree-20140225; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP937614.RAAkGweUgdQvnoU6ffcYf8CYfVYSxsZW8MTld-Qm-W__o130_publicationInfo { this: dcterms:created "2014-10-02T12:41:34+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }