@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP833260.RAjFvDnTTSdiB7FSw7B3tTjtR9VWP2F9yINss6T4nNV_8
> .
@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:NP833260.RAjFvDnTTSdiB7FSw7B3tTjtR9VWP2F9yINss6T4nNV_8130_head
{
this:
np:hasAssertion
dgn-np:NP833260.RAjFvDnTTSdiB7FSw7B3tTjtR9VWP2F9yINss6T4nNV_8130_assertion
;
np:hasProvenance
dgn-np:NP833260.RAjFvDnTTSdiB7FSw7B3tTjtR9VWP2F9yINss6T4nNV_8130_provenance
;
np:hasPublicationInfo
dgn-np:NP833260.RAjFvDnTTSdiB7FSw7B3tTjtR9VWP2F9yINss6T4nNV_8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP833260.RAjFvDnTTSdiB7FSw7B3tTjtR9VWP2F9yINss6T4nNV_8130_assertion
a
np:Assertion
.
dgn-np:NP833260.RAjFvDnTTSdiB7FSw7B3tTjtR9VWP2F9yINss6T4nNV_8130_provenance
a
np:Provenance
.
dgn-np:NP833260.RAjFvDnTTSdiB7FSw7B3tTjtR9VWP2F9yINss6T4nNV_8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP833260.RAjFvDnTTSdiB7FSw7B3tTjtR9VWP2F9yINss6T4nNV_8130_assertion
{
miriam-gene:152
a
ncit:C16612
.
lld:C0009806
a
ncit:C7057
.
dgn-gda:DGNa807889dd18a3c7c18310a66b5330da3
sio:SIO_000628
miriam-gene:152
,
lld:C0009806
;
a
sio:SIO_001121
.
}
dgn-np:NP833260.RAjFvDnTTSdiB7FSw7B3tTjtR9VWP2F9yINss6T4nNV_8130_provenance
{
dgn-np:NP833260.RAjFvDnTTSdiB7FSw7B3tTjtR9VWP2F9yINss6T4nNV_8130_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: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:NP833260.RAjFvDnTTSdiB7FSw7B3tTjtR9VWP2F9yINss6T4nNV_8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:30+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" .
}