@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP505161.RAAPOwrRfJ6JhyMei_9ezi2ZbrNicsNxxwk2sDrmsv55k
> .
@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:NP505161.RAAPOwrRfJ6JhyMei_9ezi2ZbrNicsNxxwk2sDrmsv55k130_head
{
this:
np:hasAssertion
dgn-np:NP505161.RAAPOwrRfJ6JhyMei_9ezi2ZbrNicsNxxwk2sDrmsv55k130_assertion
;
np:hasProvenance
dgn-np:NP505161.RAAPOwrRfJ6JhyMei_9ezi2ZbrNicsNxxwk2sDrmsv55k130_provenance
;
np:hasPublicationInfo
dgn-np:NP505161.RAAPOwrRfJ6JhyMei_9ezi2ZbrNicsNxxwk2sDrmsv55k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP505161.RAAPOwrRfJ6JhyMei_9ezi2ZbrNicsNxxwk2sDrmsv55k130_assertion
a
np:Assertion
.
dgn-np:NP505161.RAAPOwrRfJ6JhyMei_9ezi2ZbrNicsNxxwk2sDrmsv55k130_provenance
a
np:Provenance
.
dgn-np:NP505161.RAAPOwrRfJ6JhyMei_9ezi2ZbrNicsNxxwk2sDrmsv55k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP505161.RAAPOwrRfJ6JhyMei_9ezi2ZbrNicsNxxwk2sDrmsv55k130_assertion
{
miriam-gene:11331
a
ncit:C16612
.
lld:C0004352
a
ncit:C7057
.
dgn-gda:DGN10aa6555cc9df250f4ca9a1695b3ad9c
sio:SIO_000628
miriam-gene:11331
,
lld:C0004352
;
a
sio:SIO_001121
.
}
dgn-np:NP505161.RAAPOwrRfJ6JhyMei_9ezi2ZbrNicsNxxwk2sDrmsv55k130_provenance
{
dgn-np:NP505161.RAAPOwrRfJ6JhyMei_9ezi2ZbrNicsNxxwk2sDrmsv55k130_assertion
dcterms:description
"[Given the recent findings regarding the association between alexithymia and Autism Spectrum Disorder (ASD) and the accumulating evidence for the presence of the Broader Autism Phenotype (BAP) in relatives of individuals with ASD, we further explored the construct of alexithymia in parents of children with ASD as a potential part of the BAP.]. 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:18473159
;
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:NP505161.RAAPOwrRfJ6JhyMei_9ezi2ZbrNicsNxxwk2sDrmsv55k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:01+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" .
}