@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP734048.RAhaVDIirZyJBWA4MNXNBoFEhJIR0W266hohTajpKG_So
> .
@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:NP734048.RAhaVDIirZyJBWA4MNXNBoFEhJIR0W266hohTajpKG_So130_head
{
this:
np:hasAssertion
dgn-np:NP734048.RAhaVDIirZyJBWA4MNXNBoFEhJIR0W266hohTajpKG_So130_assertion
;
np:hasProvenance
dgn-np:NP734048.RAhaVDIirZyJBWA4MNXNBoFEhJIR0W266hohTajpKG_So130_provenance
;
np:hasPublicationInfo
dgn-np:NP734048.RAhaVDIirZyJBWA4MNXNBoFEhJIR0W266hohTajpKG_So130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP734048.RAhaVDIirZyJBWA4MNXNBoFEhJIR0W266hohTajpKG_So130_assertion
a
np:Assertion
.
dgn-np:NP734048.RAhaVDIirZyJBWA4MNXNBoFEhJIR0W266hohTajpKG_So130_provenance
a
np:Provenance
.
dgn-np:NP734048.RAhaVDIirZyJBWA4MNXNBoFEhJIR0W266hohTajpKG_So130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP734048.RAhaVDIirZyJBWA4MNXNBoFEhJIR0W266hohTajpKG_So130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0023015
a
ncit:C7057
.
dgn-gda:DGNd6628a19ba5bb19a8bb4f0fbc19eabd7
sio:SIO_000628
miriam-gene:1080
,
lld:C0023015
;
a
sio:SIO_001121
.
}
dgn-np:NP734048.RAhaVDIirZyJBWA4MNXNBoFEhJIR0W266hohTajpKG_So130_provenance
{
dgn-np:NP734048.RAhaVDIirZyJBWA4MNXNBoFEhJIR0W266hohTajpKG_So130_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-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:NP734048.RAhaVDIirZyJBWA4MNXNBoFEhJIR0W266hohTajpKG_So130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:25+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" .
}