@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:NP363490.RAO-kH78NoPKyRl_I9n4-u951tnx_TPGUOjBuJnybIhgs130_head { this: np:hasAssertion dgn-np:NP363490.RAO-kH78NoPKyRl_I9n4-u951tnx_TPGUOjBuJnybIhgs130_assertion; np:hasProvenance dgn-np:NP363490.RAO-kH78NoPKyRl_I9n4-u951tnx_TPGUOjBuJnybIhgs130_provenance; np:hasPublicationInfo dgn-np:NP363490.RAO-kH78NoPKyRl_I9n4-u951tnx_TPGUOjBuJnybIhgs130_publicationInfo; a np:Nanopublication . dgn-np:NP363490.RAO-kH78NoPKyRl_I9n4-u951tnx_TPGUOjBuJnybIhgs130_assertion a np:Assertion . dgn-np:NP363490.RAO-kH78NoPKyRl_I9n4-u951tnx_TPGUOjBuJnybIhgs130_provenance a np:Provenance . dgn-np:NP363490.RAO-kH78NoPKyRl_I9n4-u951tnx_TPGUOjBuJnybIhgs130_publicationInfo a np:PublicationInfo . } dgn-np:NP363490.RAO-kH78NoPKyRl_I9n4-u951tnx_TPGUOjBuJnybIhgs130_assertion { miriam-gene:93986 a ncit:C16612 . lld:C0037822 a ncit:C7057 . dgn-gda:DGN32a2023de4a4ec5f9cc11de1da4fac30 sio:SIO_000628 miriam-gene:93986, lld:C0037822; a sio:SIO_001121 . } dgn-np:NP363490.RAO-kH78NoPKyRl_I9n4-u951tnx_TPGUOjBuJnybIhgs130_provenance { dgn-np:NP363490.RAO-kH78NoPKyRl_I9n4-u951tnx_TPGUOjBuJnybIhgs130_assertion dcterms:description "[After completing this paper, readers should be able to (a) identify key epidemiological findings for the three speech phenotypes that were discussed (DAS, speech delay, and stuttering); (b) summarize the findings of the behavioral genetic studies of speech disorders that were presented; (c) identify four specific challenges that may impede future molecular genetic studies of these phenotypes; (d) describe the methodological sequence that led to the discovery of the FOXP2 gene; and (e) summarize the two research strategies that were presented to potentially reduce sample heterogeneity for future molecular genetics research.]. 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:12160352; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP363490.RAO-kH78NoPKyRl_I9n4-u951tnx_TPGUOjBuJnybIhgs130_publicationInfo { this: dcterms:created "2016-05-13T12:44:30+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 "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }