@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP176963.RAupWZXXaydrD_Kv31aWWVxseIfMi2Jtnl9SZux3BJids
> .
@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:NP176963.RAupWZXXaydrD_Kv31aWWVxseIfMi2Jtnl9SZux3BJids130_head
{
this:
np:hasAssertion
dgn-np:NP176963.RAupWZXXaydrD_Kv31aWWVxseIfMi2Jtnl9SZux3BJids130_assertion
;
np:hasProvenance
dgn-np:NP176963.RAupWZXXaydrD_Kv31aWWVxseIfMi2Jtnl9SZux3BJids130_provenance
;
np:hasPublicationInfo
dgn-np:NP176963.RAupWZXXaydrD_Kv31aWWVxseIfMi2Jtnl9SZux3BJids130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP176963.RAupWZXXaydrD_Kv31aWWVxseIfMi2Jtnl9SZux3BJids130_assertion
a
np:Assertion
.
dgn-np:NP176963.RAupWZXXaydrD_Kv31aWWVxseIfMi2Jtnl9SZux3BJids130_provenance
a
np:Provenance
.
dgn-np:NP176963.RAupWZXXaydrD_Kv31aWWVxseIfMi2Jtnl9SZux3BJids130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP176963.RAupWZXXaydrD_Kv31aWWVxseIfMi2Jtnl9SZux3BJids130_assertion
{
miriam-gene:7132
a
ncit:C16612
.
lld:C0038013
a
ncit:C7057
.
dgn-gda:DGNada02bd4e0a1d16d16e9df9ac7ecf433
sio:SIO_000628
miriam-gene:7132
,
lld:C0038013
;
a
sio:SIO_001121
.
}
dgn-np:NP176963.RAupWZXXaydrD_Kv31aWWVxseIfMi2Jtnl9SZux3BJids130_provenance
{
dgn-np:NP176963.RAupWZXXaydrD_Kv31aWWVxseIfMi2Jtnl9SZux3BJids130_assertion
dcterms:description
"[In view of the previously reported associations of TNFRSF1A with AS, in Caucasians and Chinese, and the biological plausibility of this candidate gene, replication of this finding in well powered studies is clearly indicated.]. 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:22272576
;
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:NP176963.RAupWZXXaydrD_Kv31aWWVxseIfMi2Jtnl9SZux3BJids130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:35+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" .
}