@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP49151.RA_JJgmmliHsa4W0qR0n2c39BBXS9nh-TeHhzN23XsfqY
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP49151.RA_JJgmmliHsa4W0qR0n2c39BBXS9nh-TeHhzN23XsfqY130_assertion
;
np:hasProvenance
dgn-np:NP49151.RA_JJgmmliHsa4W0qR0n2c39BBXS9nh-TeHhzN23XsfqY130_provenance
;
np:hasPublicationInfo
dgn-np:NP49151.RA_JJgmmliHsa4W0qR0n2c39BBXS9nh-TeHhzN23XsfqY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP49151.RA_JJgmmliHsa4W0qR0n2c39BBXS9nh-TeHhzN23XsfqY130_assertion
a
np:Assertion
.
dgn-np:NP49151.RA_JJgmmliHsa4W0qR0n2c39BBXS9nh-TeHhzN23XsfqY130_provenance
a
np:Provenance
.
dgn-np:NP49151.RA_JJgmmliHsa4W0qR0n2c39BBXS9nh-TeHhzN23XsfqY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP49151.RA_JJgmmliHsa4W0qR0n2c39BBXS9nh-TeHhzN23XsfqY130_assertion
{
miriam-gene:150
a
ncit:C16612
.
lld:C0017178
a
ncit:C7057
.
dgn-gda:DGNfa8803af1a2783e43099c68fa7173884
sio:SIO_000628
miriam-gene:150
,
lld:C0017178
;
a
sio:SIO_001122
.
}
dgn-np:NP49151.RA_JJgmmliHsa4W0qR0n2c39BBXS9nh-TeHhzN23XsfqY130_provenance
{
dgn-np:NP49151.RA_JJgmmliHsa4W0qR0n2c39BBXS9nh-TeHhzN23XsfqY130_assertion
dcterms:description
"[ Functionally distinct alpha(2A) and alpha(2C) adrenoceptor and serotonin transporter polymorphisms are associated with constipation and high somatic symptoms in patients with lower functional gastrointestinal disorders, although the strength of the genetic contribution to the phenotype is unclear.]. 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:15138209
;
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:NP49151.RA_JJgmmliHsa4W0qR0n2c39BBXS9nh-TeHhzN23XsfqY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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
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"v2.1.0" .
}