@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP80545.RA32DUPhdZb7LdMJjMFdhQYXx9--FOucSSVLwXtoEkcsU
> .
@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 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:NP80545.RA32DUPhdZb7LdMJjMFdhQYXx9--FOucSSVLwXtoEkcsU130_head
{
this:
np:hasAssertion
dgn-np:NP80545.RA32DUPhdZb7LdMJjMFdhQYXx9--FOucSSVLwXtoEkcsU130_assertion
;
np:hasProvenance
dgn-np:NP80545.RA32DUPhdZb7LdMJjMFdhQYXx9--FOucSSVLwXtoEkcsU130_provenance
;
np:hasPublicationInfo
dgn-np:NP80545.RA32DUPhdZb7LdMJjMFdhQYXx9--FOucSSVLwXtoEkcsU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP80545.RA32DUPhdZb7LdMJjMFdhQYXx9--FOucSSVLwXtoEkcsU130_assertion
a
np:Assertion
.
dgn-np:NP80545.RA32DUPhdZb7LdMJjMFdhQYXx9--FOucSSVLwXtoEkcsU130_provenance
a
np:Provenance
.
dgn-np:NP80545.RA32DUPhdZb7LdMJjMFdhQYXx9--FOucSSVLwXtoEkcsU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP80545.RA32DUPhdZb7LdMJjMFdhQYXx9--FOucSSVLwXtoEkcsU130_assertion
{
miriam-gene:7124
a
ncit:C16612
.
lld:C0022658
a
ncit:C7057
.
dgn-gda:DGN7d079572f2e35c1b53590ed33025d5fb
sio:SIO_000628
miriam-gene:7124
,
lld:C0022658
;
a
sio:SIO_001122
.
}
dgn-np:NP80545.RA32DUPhdZb7LdMJjMFdhQYXx9--FOucSSVLwXtoEkcsU130_provenance
{
dgn-np:NP80545.RA32DUPhdZb7LdMJjMFdhQYXx9--FOucSSVLwXtoEkcsU130_assertion
dct:description
"[Influence of patient's TNFA genotype correlated with high level of gene expression on the development of CAN was further demonstrated when the patients were stratified according to the HLA mismatches (HLA-DRB MMs).]. 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:18158121
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP80545.RA32DUPhdZb7LdMJjMFdhQYXx9--FOucSSVLwXtoEkcsU130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:39+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}