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http://rdf.disgenet.org/nanopublications.trig#NP828600.RArsd2nb_1-yssWHuemUPcvf3aKOXm0OndqwD9AqwWse4
> .
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> .
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http://www.w3.org/2001/XMLSchema#
> .
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http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
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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#
> .
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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#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
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np:hasAssertion
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np:hasProvenance
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a
np:Nanopublication
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a
np:Assertion
.
dgn-np:NP828600.RArsd2nb_1-yssWHuemUPcvf3aKOXm0OndqwD9AqwWse4130_provenance
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np:Provenance
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{
miriam-gene:3359
a
ncit:C16612
.
lld:C0022104
a
ncit:C7057
.
dgn-gda:DGN27f00a8df84d6fd088575f94a799a40a
sio:SIO_000628
miriam-gene:3359
,
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.
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dgn-np:NP828600.RArsd2nb_1-yssWHuemUPcvf3aKOXm0OndqwD9AqwWse4130_provenance
{
dgn-np:NP828600.RArsd2nb_1-yssWHuemUPcvf3aKOXm0OndqwD9AqwWse4130_assertion
dcterms:description
"[The second objective is to review pharmacogenetics in IBS, with the focus on cytochrome P-450 metabolism of drugs used in IBS, modulation of motor and sensory responses to serotonergic agents based on the 5-hydroxytryptamine (5-HT) transporter-linked polymorphic region (5-HTTLPR) and 5-HT(3) genetic variants, responses to a nonselective cannabinoid agonist (dronabinol) based on cannabinoid receptor (CNR1) and fatty acid amide hydrolase (FAAH) variation, and responses to a bile acid (sodium chenodeoxycholate) and bile acid binding (colesevelam) based on klothoβ (KLB) and fibroblast growth factor receptor 4 (FGFR4) variation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:22403795
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prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
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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 .
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dgn-np:NP828600.RArsd2nb_1-yssWHuemUPcvf3aKOXm0OndqwD9AqwWse4130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
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dgn-void:IBIGroup
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prv:usedData
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