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http://rdf.disgenet.org/nanopublications.trig#NP169994.RAYsJELbCUGuiNPle66DkUBkUDPsW539MRgRjNGI-hYrk
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP169994.RAYsJELbCUGuiNPle66DkUBkUDPsW539MRgRjNGI-hYrk130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP169994.RAYsJELbCUGuiNPle66DkUBkUDPsW539MRgRjNGI-hYrk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP169994.RAYsJELbCUGuiNPle66DkUBkUDPsW539MRgRjNGI-hYrk130_assertion
a
np:Assertion
.
dgn-np:NP169994.RAYsJELbCUGuiNPle66DkUBkUDPsW539MRgRjNGI-hYrk130_provenance
a
np:Provenance
.
dgn-np:NP169994.RAYsJELbCUGuiNPle66DkUBkUDPsW539MRgRjNGI-hYrk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP169994.RAYsJELbCUGuiNPle66DkUBkUDPsW539MRgRjNGI-hYrk130_assertion
{
miriam-gene:93986
a
ncit:C16612
.
lld:C0023015
a
ncit:C7057
.
dgn-gda:DGN589044751a7e0a9669435df99fc79563
sio:SIO_000628
miriam-gene:93986
,
lld:C0023015
;
a
sio:SIO_001121
.
}
dgn-np:NP169994.RAYsJELbCUGuiNPle66DkUBkUDPsW539MRgRjNGI-hYrk130_provenance
{
dgn-np:NP169994.RAYsJELbCUGuiNPle66DkUBkUDPsW539MRgRjNGI-hYrk130_assertion
dcterms:description
"[For example, rare protein-coding mutations of the FOXP2 transcription factor cause severe problems with sequencing of speech sounds, while common genetic risk variants of small effect size in genes like CNTNAP2, ATP2C2 and CMIP are associated with typical forms of language impairment.]. 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:23228431
;
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 .
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dgn-np:NP169994.RAYsJELbCUGuiNPle66DkUBkUDPsW539MRgRjNGI-hYrk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:32+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
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pav:authoredBy
<
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> , <
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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
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"v2.1.0" .
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