@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP207275.RAO50CWfBfJJnQDVfLVhqITCl6v93L_JTx_nstgEksaWU
> .
@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:NP207275.RAO50CWfBfJJnQDVfLVhqITCl6v93L_JTx_nstgEksaWU130_head
{
this:
np:hasAssertion
dgn-np:NP207275.RAO50CWfBfJJnQDVfLVhqITCl6v93L_JTx_nstgEksaWU130_assertion
;
np:hasProvenance
dgn-np:NP207275.RAO50CWfBfJJnQDVfLVhqITCl6v93L_JTx_nstgEksaWU130_provenance
;
np:hasPublicationInfo
dgn-np:NP207275.RAO50CWfBfJJnQDVfLVhqITCl6v93L_JTx_nstgEksaWU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP207275.RAO50CWfBfJJnQDVfLVhqITCl6v93L_JTx_nstgEksaWU130_assertion
a
np:Assertion
.
dgn-np:NP207275.RAO50CWfBfJJnQDVfLVhqITCl6v93L_JTx_nstgEksaWU130_provenance
a
np:Provenance
.
dgn-np:NP207275.RAO50CWfBfJJnQDVfLVhqITCl6v93L_JTx_nstgEksaWU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP207275.RAO50CWfBfJJnQDVfLVhqITCl6v93L_JTx_nstgEksaWU130_assertion
{
miriam-gene:3106
a
ncit:C16612
.
lld:C0033860
a
ncit:C7057
.
dgn-gda:DGNf06f3f135c9c8a573bbb327713d31a10
sio:SIO_000628
miriam-gene:3106
,
lld:C0033860
;
a
sio:SIO_001121
.
}
dgn-np:NP207275.RAO50CWfBfJJnQDVfLVhqITCl6v93L_JTx_nstgEksaWU130_provenance
{
dgn-np:NP207275.RAO50CWfBfJJnQDVfLVhqITCl6v93L_JTx_nstgEksaWU130_assertion
dcterms:description
"[Further clarification of these possibilities is likely to depend primarily on understanding the role of genes within the MHC in predisposing to comparatively more homogeneous diseases, such as psoriasis and ankylosing spondylitis, before the mechanisms operating in PsA can be analysed and better understood.]. 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:8076387
;
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:NP207275.RAO50CWfBfJJnQDVfLVhqITCl6v93L_JTx_nstgEksaWU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:54+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" .
}