@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP497520.RAfwmR8thBuVUvXnFtLPw288pMDC2YdoSqArpfzUgjMzw
> .
@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:NP497520.RAfwmR8thBuVUvXnFtLPw288pMDC2YdoSqArpfzUgjMzw130_head
{
this:
np:hasAssertion
dgn-np:NP497520.RAfwmR8thBuVUvXnFtLPw288pMDC2YdoSqArpfzUgjMzw130_assertion
;
np:hasProvenance
dgn-np:NP497520.RAfwmR8thBuVUvXnFtLPw288pMDC2YdoSqArpfzUgjMzw130_provenance
;
np:hasPublicationInfo
dgn-np:NP497520.RAfwmR8thBuVUvXnFtLPw288pMDC2YdoSqArpfzUgjMzw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP497520.RAfwmR8thBuVUvXnFtLPw288pMDC2YdoSqArpfzUgjMzw130_assertion
a
np:Assertion
.
dgn-np:NP497520.RAfwmR8thBuVUvXnFtLPw288pMDC2YdoSqArpfzUgjMzw130_provenance
a
np:Provenance
.
dgn-np:NP497520.RAfwmR8thBuVUvXnFtLPw288pMDC2YdoSqArpfzUgjMzw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP497520.RAfwmR8thBuVUvXnFtLPw288pMDC2YdoSqArpfzUgjMzw130_assertion
{
miriam-gene:7133
a
ncit:C16612
.
lld:C0001144
a
ncit:C7057
.
dgn-gda:DGN6c4413794ec1b9c21dc1e086efe496b2
sio:SIO_000628
miriam-gene:7133
,
lld:C0001144
;
a
sio:SIO_001121
.
}
dgn-np:NP497520.RAfwmR8thBuVUvXnFtLPw288pMDC2YdoSqArpfzUgjMzw130_provenance
{
dgn-np:NP497520.RAfwmR8thBuVUvXnFtLPw288pMDC2YdoSqArpfzUgjMzw130_assertion
dcterms:description
"[The polymerase chain reaction restriction fragment length polymorphism technique was adopted to analyze the single-nucleotide polymorphisms of the TNFR2 M196R and TLR2 Arg753Gln gene, and to examine the association between acne vulgaris and the polymorphisms in the TNFR2 M196R as well as TLR2 Arg753Gln gene.]. 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:20861605
;
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:NP497520.RAfwmR8thBuVUvXnFtLPw288pMDC2YdoSqArpfzUgjMzw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:57+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" .
}