@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP43887.RAGPcxMTTbwC4Zrx3P06eJn0UX7BuPObl-3n9z5uVcKD0
> .
@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/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@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/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP43887.RAGPcxMTTbwC4Zrx3P06eJn0UX7BuPObl-3n9z5uVcKD0130_head
{
this:
np:hasAssertion
dgn-np:NP43887.RAGPcxMTTbwC4Zrx3P06eJn0UX7BuPObl-3n9z5uVcKD0130_assertion
;
np:hasProvenance
dgn-np:NP43887.RAGPcxMTTbwC4Zrx3P06eJn0UX7BuPObl-3n9z5uVcKD0130_provenance
;
np:hasPublicationInfo
dgn-np:NP43887.RAGPcxMTTbwC4Zrx3P06eJn0UX7BuPObl-3n9z5uVcKD0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP43887.RAGPcxMTTbwC4Zrx3P06eJn0UX7BuPObl-3n9z5uVcKD0130_assertion
a
np:Assertion
.
dgn-np:NP43887.RAGPcxMTTbwC4Zrx3P06eJn0UX7BuPObl-3n9z5uVcKD0130_provenance
a
np:Provenance
.
dgn-np:NP43887.RAGPcxMTTbwC4Zrx3P06eJn0UX7BuPObl-3n9z5uVcKD0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP43887.RAGPcxMTTbwC4Zrx3P06eJn0UX7BuPObl-3n9z5uVcKD0130_assertion
{
miriam-gene:93986
a
ncit:C16612
.
lld:C0004352
a
ncit:C7057
.
dgn-gda:DGN82df4dbcd620c1747c2e1cd57b44c258
sio:SIO_000628
miriam-gene:93986
,
lld:C0004352
;
a
sio:SIO_001122
.
}
dgn-np:NP43887.RAGPcxMTTbwC4Zrx3P06eJn0UX7BuPObl-3n9z5uVcKD0130_provenance
{
dgn-np:NP43887.RAGPcxMTTbwC4Zrx3P06eJn0UX7BuPObl-3n9z5uVcKD0130_assertion
dcterms:description
"[Because of the chromosomal location of FOXP2 (7q31) and the putative implication of the 7q31 region both in autistic and in language disorders (a feature of AD), it has been hypothesized that FOXP2 may be implicated in the pathophysiology of AD.]. 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:12655497
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP43887.RAGPcxMTTbwC4Zrx3P06eJn0UX7BuPObl-3n9z5uVcKD0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:20+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:disgenetrdf
;
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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}