@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP86472.RA2AxS8ydcl1Zt5wuNChsG84S9y1LXMTPC5VOyudazGVY
> .
@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:NP86472.RA2AxS8ydcl1Zt5wuNChsG84S9y1LXMTPC5VOyudazGVY130_head
{
this:
np:hasAssertion
dgn-np:NP86472.RA2AxS8ydcl1Zt5wuNChsG84S9y1LXMTPC5VOyudazGVY130_assertion
;
np:hasProvenance
dgn-np:NP86472.RA2AxS8ydcl1Zt5wuNChsG84S9y1LXMTPC5VOyudazGVY130_provenance
;
np:hasPublicationInfo
dgn-np:NP86472.RA2AxS8ydcl1Zt5wuNChsG84S9y1LXMTPC5VOyudazGVY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP86472.RA2AxS8ydcl1Zt5wuNChsG84S9y1LXMTPC5VOyudazGVY130_assertion
a
np:Assertion
.
dgn-np:NP86472.RA2AxS8ydcl1Zt5wuNChsG84S9y1LXMTPC5VOyudazGVY130_provenance
a
np:Provenance
.
dgn-np:NP86472.RA2AxS8ydcl1Zt5wuNChsG84S9y1LXMTPC5VOyudazGVY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP86472.RA2AxS8ydcl1Zt5wuNChsG84S9y1LXMTPC5VOyudazGVY130_assertion
{
miriam-gene:3356
a
ncit:C16612
.
lld:C0033931
a
ncit:C7057
.
dgn-gda:DGN045627e67ead649b786c9ac175b3acab
sio:SIO_000628
miriam-gene:3356
,
lld:C0033931
;
a
sio:SIO_001122
.
}
dgn-np:NP86472.RA2AxS8ydcl1Zt5wuNChsG84S9y1LXMTPC5VOyudazGVY130_provenance
{
dgn-np:NP86472.RA2AxS8ydcl1Zt5wuNChsG84S9y1LXMTPC5VOyudazGVY130_assertion
dcterms:description
"[This study finds association of SNPs in HTR2A, SERPINA6, and TPH2 with somatic symptoms implicating them as potentially important in the shared genetic component to functional somatic syndromes, although replication is required.]. 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:20403506
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP86472.RA2AxS8ydcl1Zt5wuNChsG84S9y1LXMTPC5VOyudazGVY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:42+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" .
}