@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP854839.RA_SKSieMiaJ95U1WAjV8tRziTKnZZ-ZXMKqi2zuZRumY
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP854839.RA_SKSieMiaJ95U1WAjV8tRziTKnZZ-ZXMKqi2zuZRumY130_head
{
this:
np:hasAssertion
dgn-np:NP854839.RA_SKSieMiaJ95U1WAjV8tRziTKnZZ-ZXMKqi2zuZRumY130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP854839.RA_SKSieMiaJ95U1WAjV8tRziTKnZZ-ZXMKqi2zuZRumY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP854839.RA_SKSieMiaJ95U1WAjV8tRziTKnZZ-ZXMKqi2zuZRumY130_assertion
a
np:Assertion
.
dgn-np:NP854839.RA_SKSieMiaJ95U1WAjV8tRziTKnZZ-ZXMKqi2zuZRumY130_provenance
a
np:Provenance
.
dgn-np:NP854839.RA_SKSieMiaJ95U1WAjV8tRziTKnZZ-ZXMKqi2zuZRumY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP854839.RA_SKSieMiaJ95U1WAjV8tRziTKnZZ-ZXMKqi2zuZRumY130_assertion
{
miriam-gene:93986
a
ncit:C16612
.
lld:C1510586
a
ncit:C7057
.
dgn-gda:DGN47dfda83edd240b9c611ed542503c0d7
sio:SIO_000628
miriam-gene:93986
,
lld:C1510586
;
a
sio:SIO_001121
.
}
dgn-np:NP854839.RA_SKSieMiaJ95U1WAjV8tRziTKnZZ-ZXMKqi2zuZRumY130_provenance
{
dgn-np:NP854839.RA_SKSieMiaJ95U1WAjV8tRziTKnZZ-ZXMKqi2zuZRumY130_assertion
dcterms:description
"[CNTNAP2 is known to be involved in the cause of language and speech disorders and autism spectrum disorder and is in the same pathway as FOXP2, another important language gene, which makes it a candidate gene for causal studies speech and language disorders such as stuttering.]. 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:21108403
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP854839.RA_SKSieMiaJ95U1WAjV8tRziTKnZZ-ZXMKqi2zuZRumY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:12+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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pav:authoredBy
<
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v4.0.0.0" .
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pav:version
"v4.0.0" .
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