@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP331999.RAoPSLFoGtpPdQ_azL_lhXvfS8cwTU5fEhqiQVdLJPMDY
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP331999.RAoPSLFoGtpPdQ_azL_lhXvfS8cwTU5fEhqiQVdLJPMDY130_head
{
this:
np:hasAssertion
dgn-np:NP331999.RAoPSLFoGtpPdQ_azL_lhXvfS8cwTU5fEhqiQVdLJPMDY130_assertion
;
np:hasProvenance
dgn-np:NP331999.RAoPSLFoGtpPdQ_azL_lhXvfS8cwTU5fEhqiQVdLJPMDY130_provenance
;
np:hasPublicationInfo
dgn-np:NP331999.RAoPSLFoGtpPdQ_azL_lhXvfS8cwTU5fEhqiQVdLJPMDY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP331999.RAoPSLFoGtpPdQ_azL_lhXvfS8cwTU5fEhqiQVdLJPMDY130_assertion
a
np:Assertion
.
dgn-np:NP331999.RAoPSLFoGtpPdQ_azL_lhXvfS8cwTU5fEhqiQVdLJPMDY130_provenance
a
np:Provenance
.
dgn-np:NP331999.RAoPSLFoGtpPdQ_azL_lhXvfS8cwTU5fEhqiQVdLJPMDY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP331999.RAoPSLFoGtpPdQ_azL_lhXvfS8cwTU5fEhqiQVdLJPMDY130_assertion
{
miriam-gene:3133
a
ncit:C16612
.
lld:C0036202
a
ncit:C7057
.
dgn-gda:DGNd89a793edb15fd3ba1bf59e4127922aa
sio:SIO_000628
miriam-gene:3133
,
lld:C0036202
;
a
sio:SIO_001121
.
}
dgn-np:NP331999.RAoPSLFoGtpPdQ_azL_lhXvfS8cwTU5fEhqiQVdLJPMDY130_provenance
{
dgn-np:NP331999.RAoPSLFoGtpPdQ_azL_lhXvfS8cwTU5fEhqiQVdLJPMDY130_assertion
dcterms:description
"[In addition, the results allow the conclusion to be drawn that disease course associated haplotypes in sarcoidosis are highly probable and that further investigation of polymorphisms in the MHC gene region holds the potential of defining prognostic markers.]. 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:11587099
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP331999.RAoPSLFoGtpPdQ_azL_lhXvfS8cwTU5fEhqiQVdLJPMDY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:16+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}