@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP440678.RAogojNyjxVI7Yf8qkHrRi4PornBy6Cv6OaDPbaLZrjsk
> .
@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:NP440678.RAogojNyjxVI7Yf8qkHrRi4PornBy6Cv6OaDPbaLZrjsk130_head
{
this:
np:hasAssertion
dgn-np:NP440678.RAogojNyjxVI7Yf8qkHrRi4PornBy6Cv6OaDPbaLZrjsk130_assertion
;
np:hasProvenance
dgn-np:NP440678.RAogojNyjxVI7Yf8qkHrRi4PornBy6Cv6OaDPbaLZrjsk130_provenance
;
np:hasPublicationInfo
dgn-np:NP440678.RAogojNyjxVI7Yf8qkHrRi4PornBy6Cv6OaDPbaLZrjsk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP440678.RAogojNyjxVI7Yf8qkHrRi4PornBy6Cv6OaDPbaLZrjsk130_assertion
a
np:Assertion
.
dgn-np:NP440678.RAogojNyjxVI7Yf8qkHrRi4PornBy6Cv6OaDPbaLZrjsk130_provenance
a
np:Provenance
.
dgn-np:NP440678.RAogojNyjxVI7Yf8qkHrRi4PornBy6Cv6OaDPbaLZrjsk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP440678.RAogojNyjxVI7Yf8qkHrRi4PornBy6Cv6OaDPbaLZrjsk130_assertion
{
miriam-gene:7132
a
ncit:C16612
.
lld:C0038013
a
ncit:C7057
.
dgn-gda:DGN3f9c61dc6043374b5274c151aff4cfeb
sio:SIO_000628
miriam-gene:7132
,
lld:C0038013
;
a
sio:SIO_001121
.
}
dgn-np:NP440678.RAogojNyjxVI7Yf8qkHrRi4PornBy6Cv6OaDPbaLZrjsk130_provenance
{
dgn-np:NP440678.RAogojNyjxVI7Yf8qkHrRi4PornBy6Cv6OaDPbaLZrjsk130_assertion
dcterms:description
"[The study results demonstrate for the first time that genetic polymorphisms in STAT3, TNFRSF1A and 2p15 are associated with AS in Han Chinese, suggesting common pathogenic mechanisms for the disease in Chinese and Caucasian European populations.]. 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:21068102
;
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:NP440678.RAogojNyjxVI7Yf8qkHrRi4PornBy6Cv6OaDPbaLZrjsk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:20+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" .
}