@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP509018.RACgi9nSgYgoYRCG3Cog3LLQrMbvoyZQTHMNdZwsHPSFI
> .
@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:NP509018.RACgi9nSgYgoYRCG3Cog3LLQrMbvoyZQTHMNdZwsHPSFI130_head
{
this:
np:hasAssertion
dgn-np:NP509018.RACgi9nSgYgoYRCG3Cog3LLQrMbvoyZQTHMNdZwsHPSFI130_assertion
;
np:hasProvenance
dgn-np:NP509018.RACgi9nSgYgoYRCG3Cog3LLQrMbvoyZQTHMNdZwsHPSFI130_provenance
;
np:hasPublicationInfo
dgn-np:NP509018.RACgi9nSgYgoYRCG3Cog3LLQrMbvoyZQTHMNdZwsHPSFI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP509018.RACgi9nSgYgoYRCG3Cog3LLQrMbvoyZQTHMNdZwsHPSFI130_assertion
a
np:Assertion
.
dgn-np:NP509018.RACgi9nSgYgoYRCG3Cog3LLQrMbvoyZQTHMNdZwsHPSFI130_provenance
a
np:Provenance
.
dgn-np:NP509018.RACgi9nSgYgoYRCG3Cog3LLQrMbvoyZQTHMNdZwsHPSFI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP509018.RACgi9nSgYgoYRCG3Cog3LLQrMbvoyZQTHMNdZwsHPSFI130_assertion
{
miriam-gene:23158
a
ncit:C16612
.
lld:C0003873
a
ncit:C7057
.
dgn-gda:DGN9d13681073effcd7d8464237cacf3c0f
sio:SIO_000628
miriam-gene:23158
,
lld:C0003873
;
a
sio:SIO_001121
.
}
dgn-np:NP509018.RACgi9nSgYgoYRCG3Cog3LLQrMbvoyZQTHMNdZwsHPSFI130_provenance
{
dgn-np:NP509018.RACgi9nSgYgoYRCG3Cog3LLQrMbvoyZQTHMNdZwsHPSFI130_assertion
dcterms:description
"[We suggest that the C3435T MDR1 polymorphism is not an important genetic risk factor for RA susceptibility, but that this polymorphism may have an influence on the activity of the disease and its response to therapy with disease-modifying antirheumatic drugs.]. 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:15487808
;
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:NP509018.RACgi9nSgYgoYRCG3Cog3LLQrMbvoyZQTHMNdZwsHPSFI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:03+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" .
}