@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1077530.RAq4G68PeobxBgt3XOkJPc9Psgkds9GIPu94TWu1Kmb58
> .
@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:NP1077530.RAq4G68PeobxBgt3XOkJPc9Psgkds9GIPu94TWu1Kmb58130_head
{
this:
np:hasAssertion
dgn-np:NP1077530.RAq4G68PeobxBgt3XOkJPc9Psgkds9GIPu94TWu1Kmb58130_assertion
;
np:hasProvenance
dgn-np:NP1077530.RAq4G68PeobxBgt3XOkJPc9Psgkds9GIPu94TWu1Kmb58130_provenance
;
np:hasPublicationInfo
dgn-np:NP1077530.RAq4G68PeobxBgt3XOkJPc9Psgkds9GIPu94TWu1Kmb58130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1077530.RAq4G68PeobxBgt3XOkJPc9Psgkds9GIPu94TWu1Kmb58130_assertion
a
np:Assertion
.
dgn-np:NP1077530.RAq4G68PeobxBgt3XOkJPc9Psgkds9GIPu94TWu1Kmb58130_provenance
a
np:Provenance
.
dgn-np:NP1077530.RAq4G68PeobxBgt3XOkJPc9Psgkds9GIPu94TWu1Kmb58130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1077530.RAq4G68PeobxBgt3XOkJPc9Psgkds9GIPu94TWu1Kmb58130_assertion
{
miriam-gene:51008
a
ncit:C16612
.
lld:C0010054
a
ncit:C7057
.
dgn-gda:DGN8a7024fd94512f9358c12b45f5025ec0
sio:SIO_000628
miriam-gene:51008
,
lld:C0010054
;
a
sio:SIO_001121
.
}
dgn-np:NP1077530.RAq4G68PeobxBgt3XOkJPc9Psgkds9GIPu94TWu1Kmb58130_provenance
{
dgn-np:NP1077530.RAq4G68PeobxBgt3XOkJPc9Psgkds9GIPu94TWu1Kmb58130_assertion
dcterms:description
"[The deletion variant allele of the NFKB1 - 94ins/delATTG promoter polymorphism leads to lower transcript levels of the p50 subunit, and the variant allele has been associated with the risk of several inflammatory diseases as well as coronary heart disease where inflammation is important in the pathogenesis.]. 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:23671649
;
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:NP1077530.RAq4G68PeobxBgt3XOkJPc9Psgkds9GIPu94TWu1Kmb58130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:54+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: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" .
}