@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP749617.RAFsFKcAHnejgjJ3x78UUnbC_kwjuY0vrQoQTEZhbelCY
> .
@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:NP749617.RAFsFKcAHnejgjJ3x78UUnbC_kwjuY0vrQoQTEZhbelCY130_head
{
this:
np:hasAssertion
dgn-np:NP749617.RAFsFKcAHnejgjJ3x78UUnbC_kwjuY0vrQoQTEZhbelCY130_assertion
;
np:hasProvenance
dgn-np:NP749617.RAFsFKcAHnejgjJ3x78UUnbC_kwjuY0vrQoQTEZhbelCY130_provenance
;
np:hasPublicationInfo
dgn-np:NP749617.RAFsFKcAHnejgjJ3x78UUnbC_kwjuY0vrQoQTEZhbelCY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP749617.RAFsFKcAHnejgjJ3x78UUnbC_kwjuY0vrQoQTEZhbelCY130_assertion
a
np:Assertion
.
dgn-np:NP749617.RAFsFKcAHnejgjJ3x78UUnbC_kwjuY0vrQoQTEZhbelCY130_provenance
a
np:Provenance
.
dgn-np:NP749617.RAFsFKcAHnejgjJ3x78UUnbC_kwjuY0vrQoQTEZhbelCY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP749617.RAFsFKcAHnejgjJ3x78UUnbC_kwjuY0vrQoQTEZhbelCY130_assertion
{
miriam-gene:26047
a
ncit:C16612
.
lld:C0040517
a
ncit:C7057
.
dgn-gda:DGNaf9df317a773621be5d2df1927ea95b7
sio:SIO_000628
miriam-gene:26047
,
lld:C0040517
;
a
sio:SIO_001121
.
}
dgn-np:NP749617.RAFsFKcAHnejgjJ3x78UUnbC_kwjuY0vrQoQTEZhbelCY130_provenance
{
dgn-np:NP749617.RAFsFKcAHnejgjJ3x78UUnbC_kwjuY0vrQoQTEZhbelCY130_assertion
dcterms:description
"[Comparison of disruptions of CNTNAP2 in patients with GTS and ASD suggests that large proximal disruptions result in either GTS or ASD, while relatively small distal disruptions may be phenotypically neutral.]. 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:19582487
;
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:NP749617.RAFsFKcAHnejgjJ3x78UUnbC_kwjuY0vrQoQTEZhbelCY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:25+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: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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}