@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP456273.RABtKE7ncKbLFjrgyfkEy9k54OGU_0Cv0UATjX2h71FM4
> .
@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:NP456273.RABtKE7ncKbLFjrgyfkEy9k54OGU_0Cv0UATjX2h71FM4130_head
{
this:
np:hasAssertion
dgn-np:NP456273.RABtKE7ncKbLFjrgyfkEy9k54OGU_0Cv0UATjX2h71FM4130_assertion
;
np:hasProvenance
dgn-np:NP456273.RABtKE7ncKbLFjrgyfkEy9k54OGU_0Cv0UATjX2h71FM4130_provenance
;
np:hasPublicationInfo
dgn-np:NP456273.RABtKE7ncKbLFjrgyfkEy9k54OGU_0Cv0UATjX2h71FM4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP456273.RABtKE7ncKbLFjrgyfkEy9k54OGU_0Cv0UATjX2h71FM4130_assertion
a
np:Assertion
.
dgn-np:NP456273.RABtKE7ncKbLFjrgyfkEy9k54OGU_0Cv0UATjX2h71FM4130_provenance
a
np:Provenance
.
dgn-np:NP456273.RABtKE7ncKbLFjrgyfkEy9k54OGU_0Cv0UATjX2h71FM4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP456273.RABtKE7ncKbLFjrgyfkEy9k54OGU_0Cv0UATjX2h71FM4130_assertion
{
miriam-gene:3133
a
ncit:C16612
.
lld:C1449563
a
ncit:C7057
.
dgn-gda:DGN68f5425c8fdf11b4d5c763101ee02a52
sio:SIO_000628
miriam-gene:3133
,
lld:C1449563
;
a
sio:SIO_001121
.
}
dgn-np:NP456273.RABtKE7ncKbLFjrgyfkEy9k54OGU_0Cv0UATjX2h71FM4130_provenance
{
dgn-np:NP456273.RABtKE7ncKbLFjrgyfkEy9k54OGU_0Cv0UATjX2h71FM4130_assertion
dcterms:description
"[Therefore, the authors started their investigation with the search for MHC class 2 DQ polymorphisms in the peripheral blood of patients with DCM in parallel to the search for new interesting susceptibility loci by the use of the microarray analysis regarding genes responsible for inflammatory and autoimmune diseases.]. 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:16170686
;
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:NP456273.RABtKE7ncKbLFjrgyfkEy9k54OGU_0Cv0UATjX2h71FM4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:32+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" .
}