@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP401066.RAnkFnbqbtdcNON5VY9OL3pCcYyIGGkGRE6PzcqmfL7Do
> .
@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:NP401066.RAnkFnbqbtdcNON5VY9OL3pCcYyIGGkGRE6PzcqmfL7Do130_head
{
this:
np:hasAssertion
dgn-np:NP401066.RAnkFnbqbtdcNON5VY9OL3pCcYyIGGkGRE6PzcqmfL7Do130_assertion
;
np:hasProvenance
dgn-np:NP401066.RAnkFnbqbtdcNON5VY9OL3pCcYyIGGkGRE6PzcqmfL7Do130_provenance
;
np:hasPublicationInfo
dgn-np:NP401066.RAnkFnbqbtdcNON5VY9OL3pCcYyIGGkGRE6PzcqmfL7Do130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP401066.RAnkFnbqbtdcNON5VY9OL3pCcYyIGGkGRE6PzcqmfL7Do130_assertion
a
np:Assertion
.
dgn-np:NP401066.RAnkFnbqbtdcNON5VY9OL3pCcYyIGGkGRE6PzcqmfL7Do130_provenance
a
np:Provenance
.
dgn-np:NP401066.RAnkFnbqbtdcNON5VY9OL3pCcYyIGGkGRE6PzcqmfL7Do130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP401066.RAnkFnbqbtdcNON5VY9OL3pCcYyIGGkGRE6PzcqmfL7Do130_assertion
{
miriam-gene:6898
a
ncit:C16612
.
lld:C0013146
a
ncit:C7057
.
dgn-gda:DGN253e266f422b157b7329f586149a49f7
sio:SIO_000628
miriam-gene:6898
,
lld:C0013146
;
a
sio:SIO_001121
.
}
dgn-np:NP401066.RAnkFnbqbtdcNON5VY9OL3pCcYyIGGkGRE6PzcqmfL7Do130_provenance
{
dgn-np:NP401066.RAnkFnbqbtdcNON5VY9OL3pCcYyIGGkGRE6PzcqmfL7Do130_assertion
dcterms:description
"[Having two copies of the TAT haplotype of CRHR1 was associated with higher levels of neuroticism among maltreated children relative to nonmaltreated children, with the exception of sexually abused children and children who had experienced 3 or 4 types of abuse.]. 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:21438878
;
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:NP401066.RAnkFnbqbtdcNON5VY9OL3pCcYyIGGkGRE6PzcqmfL7Do130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:59+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" .
}