@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP881331.RAUKkeBKRrJK2OacAFhy4bh1F0h4TxpD90ewtLLjkUJdo
> .
@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/v3.0.0/void/
> .
dgn-np:NP881331.RAUKkeBKRrJK2OacAFhy4bh1F0h4TxpD90ewtLLjkUJdo130_head
{
this:
np:hasAssertion
dgn-np:NP881331.RAUKkeBKRrJK2OacAFhy4bh1F0h4TxpD90ewtLLjkUJdo130_assertion
;
np:hasProvenance
dgn-np:NP881331.RAUKkeBKRrJK2OacAFhy4bh1F0h4TxpD90ewtLLjkUJdo130_provenance
;
np:hasPublicationInfo
dgn-np:NP881331.RAUKkeBKRrJK2OacAFhy4bh1F0h4TxpD90ewtLLjkUJdo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP881331.RAUKkeBKRrJK2OacAFhy4bh1F0h4TxpD90ewtLLjkUJdo130_assertion
a
np:Assertion
.
dgn-np:NP881331.RAUKkeBKRrJK2OacAFhy4bh1F0h4TxpD90ewtLLjkUJdo130_provenance
a
np:Provenance
.
dgn-np:NP881331.RAUKkeBKRrJK2OacAFhy4bh1F0h4TxpD90ewtLLjkUJdo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP881331.RAUKkeBKRrJK2OacAFhy4bh1F0h4TxpD90ewtLLjkUJdo130_assertion
{
miriam-gene:26047
a
ncit:C16612
.
lld:C0454651
a
ncit:C7057
.
dgn-gda:DGN75ee245d4574acd6537d6a61390c79bc
sio:SIO_000628
miriam-gene:26047
,
lld:C0454651
;
a
sio:SIO_001121
.
}
dgn-np:NP881331.RAUKkeBKRrJK2OacAFhy4bh1F0h4TxpD90ewtLLjkUJdo130_provenance
{
dgn-np:NP881331.RAUKkeBKRrJK2OacAFhy4bh1F0h4TxpD90ewtLLjkUJdo130_assertion
dcterms:description
"[Common variants in contactin-associated protein-like 2 (CNTNAP2), a neurexin superfamily member, have been associated with several allied neurodevelopmental disorders, including autism and specific language impairment, and CNTNAP2 is highly expressed in frontal lobe circuits in the developing human brain.]. 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:21048216
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP881331.RAUKkeBKRrJK2OacAFhy4bh1F0h4TxpD90ewtLLjkUJdo130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:37+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}