@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP408910.RA5Qj1FOn2SsYa3aHlNcIoWTomDxEGSF_qXNquRf3E3S4
> .
@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:NP408910.RA5Qj1FOn2SsYa3aHlNcIoWTomDxEGSF_qXNquRf3E3S4130_head
{
this:
np:hasAssertion
dgn-np:NP408910.RA5Qj1FOn2SsYa3aHlNcIoWTomDxEGSF_qXNquRf3E3S4130_assertion
;
np:hasProvenance
dgn-np:NP408910.RA5Qj1FOn2SsYa3aHlNcIoWTomDxEGSF_qXNquRf3E3S4130_provenance
;
np:hasPublicationInfo
dgn-np:NP408910.RA5Qj1FOn2SsYa3aHlNcIoWTomDxEGSF_qXNquRf3E3S4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP408910.RA5Qj1FOn2SsYa3aHlNcIoWTomDxEGSF_qXNquRf3E3S4130_assertion
a
np:Assertion
.
dgn-np:NP408910.RA5Qj1FOn2SsYa3aHlNcIoWTomDxEGSF_qXNquRf3E3S4130_provenance
a
np:Provenance
.
dgn-np:NP408910.RA5Qj1FOn2SsYa3aHlNcIoWTomDxEGSF_qXNquRf3E3S4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP408910.RA5Qj1FOn2SsYa3aHlNcIoWTomDxEGSF_qXNquRf3E3S4130_assertion
{
miriam-gene:93986
a
ncit:C16612
.
lld:C0004352
a
ncit:C7057
.
dgn-gda:DGN6340512884584f7a317520fa1210cc3d
sio:SIO_000628
miriam-gene:93986
,
lld:C0004352
;
a
sio:SIO_001121
.
}
dgn-np:NP408910.RA5Qj1FOn2SsYa3aHlNcIoWTomDxEGSF_qXNquRf3E3S4130_provenance
{
dgn-np:NP408910.RA5Qj1FOn2SsYa3aHlNcIoWTomDxEGSF_qXNquRf3E3S4130_assertion
dcterms:description
"[Our patient's deletion, which is the smallest reported deletion including FOXP2, adds to the body of evidence that supports the role of FOXP2 in speech and language impairment, but not in autism.]. 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:17330859
;
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:NP408910.RA5Qj1FOn2SsYa3aHlNcIoWTomDxEGSF_qXNquRf3E3S4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:03+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" .
}