@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP62112.RAm5D2EaphFaxPVrQJ3sRHIC3b7_9bur_GCeoRfaT1WbY
> .
@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:NP62112.RAm5D2EaphFaxPVrQJ3sRHIC3b7_9bur_GCeoRfaT1WbY130_head
{
this:
np:hasAssertion
dgn-np:NP62112.RAm5D2EaphFaxPVrQJ3sRHIC3b7_9bur_GCeoRfaT1WbY130_assertion
;
np:hasProvenance
dgn-np:NP62112.RAm5D2EaphFaxPVrQJ3sRHIC3b7_9bur_GCeoRfaT1WbY130_provenance
;
np:hasPublicationInfo
dgn-np:NP62112.RAm5D2EaphFaxPVrQJ3sRHIC3b7_9bur_GCeoRfaT1WbY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP62112.RAm5D2EaphFaxPVrQJ3sRHIC3b7_9bur_GCeoRfaT1WbY130_assertion
a
np:Assertion
.
dgn-np:NP62112.RAm5D2EaphFaxPVrQJ3sRHIC3b7_9bur_GCeoRfaT1WbY130_provenance
a
np:Provenance
.
dgn-np:NP62112.RAm5D2EaphFaxPVrQJ3sRHIC3b7_9bur_GCeoRfaT1WbY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP62112.RAm5D2EaphFaxPVrQJ3sRHIC3b7_9bur_GCeoRfaT1WbY130_assertion
{
miriam-gene:7298
a
ncit:C16612
.
lld:C0003873
a
ncit:C7057
.
dgn-gda:DGN7ab909a494030526d1dde7705a6bbc40
sio:SIO_000628
miriam-gene:7298
,
lld:C0003873
;
a
sio:SIO_001122
.
}
dgn-np:NP62112.RAm5D2EaphFaxPVrQJ3sRHIC3b7_9bur_GCeoRfaT1WbY130_provenance
{
dgn-np:NP62112.RAm5D2EaphFaxPVrQJ3sRHIC3b7_9bur_GCeoRfaT1WbY130_assertion
dcterms:description
"[Thirty-four nave RA patients on supervised MTX therapy and 139 healthy controls were genotyped for A1298C and C677T polymorphism of the MTHFR gene and 5' UTR repeat and 3' UTR deletion polymorphism of the TYMS gene by polymerase chain reaction-restriction fragment length polymorphism.]. 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:18274813
;
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:NP62112.RAm5D2EaphFaxPVrQJ3sRHIC3b7_9bur_GCeoRfaT1WbY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:29+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" .
}