@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP823375.RA0pTEG1p9tLb6fRCq872WkbTh0IrS4u3h0wFXbvj_SFE
> .
@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:NP823375.RA0pTEG1p9tLb6fRCq872WkbTh0IrS4u3h0wFXbvj_SFE130_head
{
this:
np:hasAssertion
dgn-np:NP823375.RA0pTEG1p9tLb6fRCq872WkbTh0IrS4u3h0wFXbvj_SFE130_assertion
;
np:hasProvenance
dgn-np:NP823375.RA0pTEG1p9tLb6fRCq872WkbTh0IrS4u3h0wFXbvj_SFE130_provenance
;
np:hasPublicationInfo
dgn-np:NP823375.RA0pTEG1p9tLb6fRCq872WkbTh0IrS4u3h0wFXbvj_SFE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP823375.RA0pTEG1p9tLb6fRCq872WkbTh0IrS4u3h0wFXbvj_SFE130_assertion
a
np:Assertion
.
dgn-np:NP823375.RA0pTEG1p9tLb6fRCq872WkbTh0IrS4u3h0wFXbvj_SFE130_provenance
a
np:Provenance
.
dgn-np:NP823375.RA0pTEG1p9tLb6fRCq872WkbTh0IrS4u3h0wFXbvj_SFE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP823375.RA0pTEG1p9tLb6fRCq872WkbTh0IrS4u3h0wFXbvj_SFE130_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:NP823375.RA0pTEG1p9tLb6fRCq872WkbTh0IrS4u3h0wFXbvj_SFE130_provenance
{
dgn-np:NP823375.RA0pTEG1p9tLb6fRCq872WkbTh0IrS4u3h0wFXbvj_SFE130_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-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:NP823375.RA0pTEG1p9tLb6fRCq872WkbTh0IrS4u3h0wFXbvj_SFE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:24+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" .
}