@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP287263.RA-TnBLWxO5KnyuEr7XapBTQoeIuNIOqi-y4MJUeKOvH4
> .
@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:NP287263.RA-TnBLWxO5KnyuEr7XapBTQoeIuNIOqi-y4MJUeKOvH4130_head
{
this:
np:hasAssertion
dgn-np:NP287263.RA-TnBLWxO5KnyuEr7XapBTQoeIuNIOqi-y4MJUeKOvH4130_assertion
;
np:hasProvenance
dgn-np:NP287263.RA-TnBLWxO5KnyuEr7XapBTQoeIuNIOqi-y4MJUeKOvH4130_provenance
;
np:hasPublicationInfo
dgn-np:NP287263.RA-TnBLWxO5KnyuEr7XapBTQoeIuNIOqi-y4MJUeKOvH4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP287263.RA-TnBLWxO5KnyuEr7XapBTQoeIuNIOqi-y4MJUeKOvH4130_assertion
a
np:Assertion
.
dgn-np:NP287263.RA-TnBLWxO5KnyuEr7XapBTQoeIuNIOqi-y4MJUeKOvH4130_provenance
a
np:Provenance
.
dgn-np:NP287263.RA-TnBLWxO5KnyuEr7XapBTQoeIuNIOqi-y4MJUeKOvH4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP287263.RA-TnBLWxO5KnyuEr7XapBTQoeIuNIOqi-y4MJUeKOvH4130_assertion
{
miriam-gene:196527
a
ncit:C16612
.
lld:C0038013
a
ncit:C7057
.
dgn-gda:DGNdb26bcc4fce9f9978e40804ee3640050
sio:SIO_000628
miriam-gene:196527
,
lld:C0038013
;
a
sio:SIO_001121
.
}
dgn-np:NP287263.RA-TnBLWxO5KnyuEr7XapBTQoeIuNIOqi-y4MJUeKOvH4130_provenance
{
dgn-np:NP287263.RA-TnBLWxO5KnyuEr7XapBTQoeIuNIOqi-y4MJUeKOvH4130_assertion
dcterms:description
"[A recent genome-wide association study (GWAS) showed that two new susceptibility loci between EDIL3 and HAPLN1 at 5q14.3 (rs4552569) and within ANO6 at 12q12 (rs17095830) contribute to the risk of AS in Han Chinese.]. 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:23308121
;
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:NP287263.RA-TnBLWxO5KnyuEr7XapBTQoeIuNIOqi-y4MJUeKOvH4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:43+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" .
}