@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:NP392741.RA73LJy8Rgz70W08s8Dacu9s8rkUWQ8x4onCvQASswTYA130_head { this: np:hasAssertion dgn-np:NP392741.RA73LJy8Rgz70W08s8Dacu9s8rkUWQ8x4onCvQASswTYA130_assertion; np:hasProvenance dgn-np:NP392741.RA73LJy8Rgz70W08s8Dacu9s8rkUWQ8x4onCvQASswTYA130_provenance; np:hasPublicationInfo dgn-np:NP392741.RA73LJy8Rgz70W08s8Dacu9s8rkUWQ8x4onCvQASswTYA130_publicationInfo; a np:Nanopublication . dgn-np:NP392741.RA73LJy8Rgz70W08s8Dacu9s8rkUWQ8x4onCvQASswTYA130_assertion a np:Assertion . dgn-np:NP392741.RA73LJy8Rgz70W08s8Dacu9s8rkUWQ8x4onCvQASswTYA130_provenance a np:Provenance . dgn-np:NP392741.RA73LJy8Rgz70W08s8Dacu9s8rkUWQ8x4onCvQASswTYA130_publicationInfo a np:PublicationInfo . } dgn-np:NP392741.RA73LJy8Rgz70W08s8Dacu9s8rkUWQ8x4onCvQASswTYA130_assertion { miriam-gene:93986 a ncit:C16612 . lld:C0454651 a ncit:C7057 . dgn-gda:DGNb1a1aea6636a9646802cbfac12a1df02 sio:SIO_000628 miriam-gene:93986, lld:C0454651; a sio:SIO_001121 . } dgn-np:NP392741.RA73LJy8Rgz70W08s8Dacu9s8rkUWQ8x4onCvQASswTYA130_provenance { dgn-np:NP392741.RA73LJy8Rgz70W08s8Dacu9s8rkUWQ8x4onCvQASswTYA130_assertion dcterms:description "[In the present study, samples from children with SLI and their family members were used to study linkage and association of SLI to markers within and around FOXP2, and samples from 96 probands with SLI were directly sequenced for the mutation in exon 14 of FOXP2.]. 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:12721956; 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:NP392741.RA73LJy8Rgz70W08s8Dacu9s8rkUWQ8x4onCvQASswTYA130_publicationInfo { this: dcterms:created "2016-05-13T12:44:43+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" . }