@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP92224.RAI9Kw6ww3UMX-QpqPcMf_xq7P2gv8KKUaZVxD_5nnI7Q
> .
@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:NP92224.RAI9Kw6ww3UMX-QpqPcMf_xq7P2gv8KKUaZVxD_5nnI7Q130_head
{
this:
np:hasAssertion
dgn-np:NP92224.RAI9Kw6ww3UMX-QpqPcMf_xq7P2gv8KKUaZVxD_5nnI7Q130_assertion
;
np:hasProvenance
dgn-np:NP92224.RAI9Kw6ww3UMX-QpqPcMf_xq7P2gv8KKUaZVxD_5nnI7Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP92224.RAI9Kw6ww3UMX-QpqPcMf_xq7P2gv8KKUaZVxD_5nnI7Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP92224.RAI9Kw6ww3UMX-QpqPcMf_xq7P2gv8KKUaZVxD_5nnI7Q130_assertion
a
np:Assertion
.
dgn-np:NP92224.RAI9Kw6ww3UMX-QpqPcMf_xq7P2gv8KKUaZVxD_5nnI7Q130_provenance
a
np:Provenance
.
dgn-np:NP92224.RAI9Kw6ww3UMX-QpqPcMf_xq7P2gv8KKUaZVxD_5nnI7Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP92224.RAI9Kw6ww3UMX-QpqPcMf_xq7P2gv8KKUaZVxD_5nnI7Q130_assertion
{
miriam-gene:6532
a
ncit:C16612
.
lld:C0033931
a
ncit:C7057
.
dgn-gda:DGNac1dbe58868d42e8610f63852dcad418
sio:SIO_000628
miriam-gene:6532
,
lld:C0033931
;
a
sio:SIO_001122
.
}
dgn-np:NP92224.RAI9Kw6ww3UMX-QpqPcMf_xq7P2gv8KKUaZVxD_5nnI7Q130_provenance
{
dgn-np:NP92224.RAI9Kw6ww3UMX-QpqPcMf_xq7P2gv8KKUaZVxD_5nnI7Q130_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:NP92224.RAI9Kw6ww3UMX-QpqPcMf_xq7P2gv8KKUaZVxD_5nnI7Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:45+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" .
}