@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP305032.RAcTUl1W5-p5HJv6UFkIn65MfqSZ0_CUeh6ei1MOt9foA
> .
@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:NP305032.RAcTUl1W5-p5HJv6UFkIn65MfqSZ0_CUeh6ei1MOt9foA130_head
{
this:
np:hasAssertion
dgn-np:NP305032.RAcTUl1W5-p5HJv6UFkIn65MfqSZ0_CUeh6ei1MOt9foA130_assertion
;
np:hasProvenance
dgn-np:NP305032.RAcTUl1W5-p5HJv6UFkIn65MfqSZ0_CUeh6ei1MOt9foA130_provenance
;
np:hasPublicationInfo
dgn-np:NP305032.RAcTUl1W5-p5HJv6UFkIn65MfqSZ0_CUeh6ei1MOt9foA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP305032.RAcTUl1W5-p5HJv6UFkIn65MfqSZ0_CUeh6ei1MOt9foA130_assertion
a
np:Assertion
.
dgn-np:NP305032.RAcTUl1W5-p5HJv6UFkIn65MfqSZ0_CUeh6ei1MOt9foA130_provenance
a
np:Provenance
.
dgn-np:NP305032.RAcTUl1W5-p5HJv6UFkIn65MfqSZ0_CUeh6ei1MOt9foA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP305032.RAcTUl1W5-p5HJv6UFkIn65MfqSZ0_CUeh6ei1MOt9foA130_assertion
{
miriam-gene:3120
a
ncit:C16612
.
lld:C1449563
a
ncit:C7057
.
dgn-gda:DGNfea5a636971dc8ed91b870e375e5f5c9
sio:SIO_000628
miriam-gene:3120
,
lld:C1449563
;
a
sio:SIO_001121
.
}
dgn-np:NP305032.RAcTUl1W5-p5HJv6UFkIn65MfqSZ0_CUeh6ei1MOt9foA130_provenance
{
dgn-np:NP305032.RAcTUl1W5-p5HJv6UFkIn65MfqSZ0_CUeh6ei1MOt9foA130_assertion
dcterms:description
"[Typing of HLA DQB1* allele was performed using a sequence-specific primer-polymerase chain reaction technique in 22 unrelated patients with idiopathic DCM, 19 patients with myocarditis and normal left ventricular function, and 16 patients with myocarditis and impaired left ventricular function (i.e.]. 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:19127454
;
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:NP305032.RAcTUl1W5-p5HJv6UFkIn65MfqSZ0_CUeh6ei1MOt9foA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:55+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" .
}