@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP392740.RAfYkolL5O1xETZQ640CxoIl25gNq71tJ1dphXXjqCe6g
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP392740.RAfYkolL5O1xETZQ640CxoIl25gNq71tJ1dphXXjqCe6g130_head
{
this:
np:hasAssertion
dgn-np:NP392740.RAfYkolL5O1xETZQ640CxoIl25gNq71tJ1dphXXjqCe6g130_assertion
;
np:hasProvenance
dgn-np:NP392740.RAfYkolL5O1xETZQ640CxoIl25gNq71tJ1dphXXjqCe6g130_provenance
;
np:hasPublicationInfo
dgn-np:NP392740.RAfYkolL5O1xETZQ640CxoIl25gNq71tJ1dphXXjqCe6g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP392740.RAfYkolL5O1xETZQ640CxoIl25gNq71tJ1dphXXjqCe6g130_assertion
a
np:Assertion
.
dgn-np:NP392740.RAfYkolL5O1xETZQ640CxoIl25gNq71tJ1dphXXjqCe6g130_provenance
a
np:Provenance
.
dgn-np:NP392740.RAfYkolL5O1xETZQ640CxoIl25gNq71tJ1dphXXjqCe6g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP392740.RAfYkolL5O1xETZQ640CxoIl25gNq71tJ1dphXXjqCe6g130_assertion
{
miriam-gene:93986
a
ncit:C16612
.
lld:C0023015
a
ncit:C7057
.
dgn-gda:DGN0a013536c39eb8e8552f8d952f0fdac9
sio:SIO_000628
miriam-gene:93986
,
lld:C0023015
;
a
sio:SIO_001121
.
}
dgn-np:NP392740.RAfYkolL5O1xETZQ640CxoIl25gNq71tJ1dphXXjqCe6g130_provenance
{
dgn-np:NP392740.RAfYkolL5O1xETZQ640CxoIl25gNq71tJ1dphXXjqCe6g130_assertion
dcterms:description
"[No mutations were found in exon 14 of FOXP2, but strong association was found to a marker within the CFTR gene and another marker on 7q31, D7S3052, both adjacent to FOXP2, suggesting that genetic factors for regulation of common language impairment reside in the vicinity 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:NP392740.RAfYkolL5O1xETZQ640CxoIl25gNq71tJ1dphXXjqCe6g130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:43+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetv3.0rdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}