@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP174508.RA7FsK4c0NxOFSyE7kKubOxKSXO6_JmkgwRCqou5qNWSs
> .
@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:NP174508.RA7FsK4c0NxOFSyE7kKubOxKSXO6_JmkgwRCqou5qNWSs130_head
{
this:
np:hasAssertion
dgn-np:NP174508.RA7FsK4c0NxOFSyE7kKubOxKSXO6_JmkgwRCqou5qNWSs130_assertion
;
np:hasProvenance
dgn-np:NP174508.RA7FsK4c0NxOFSyE7kKubOxKSXO6_JmkgwRCqou5qNWSs130_provenance
;
np:hasPublicationInfo
dgn-np:NP174508.RA7FsK4c0NxOFSyE7kKubOxKSXO6_JmkgwRCqou5qNWSs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP174508.RA7FsK4c0NxOFSyE7kKubOxKSXO6_JmkgwRCqou5qNWSs130_assertion
a
np:Assertion
.
dgn-np:NP174508.RA7FsK4c0NxOFSyE7kKubOxKSXO6_JmkgwRCqou5qNWSs130_provenance
a
np:Provenance
.
dgn-np:NP174508.RA7FsK4c0NxOFSyE7kKubOxKSXO6_JmkgwRCqou5qNWSs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP174508.RA7FsK4c0NxOFSyE7kKubOxKSXO6_JmkgwRCqou5qNWSs130_assertion
{
miriam-gene:3552
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGNf0b312e0c7bd7db8107a4cf198fef671
sio:SIO_000628
miriam-gene:3552
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP174508.RA7FsK4c0NxOFSyE7kKubOxKSXO6_JmkgwRCqou5qNWSs130_provenance
{
dgn-np:NP174508.RA7FsK4c0NxOFSyE7kKubOxKSXO6_JmkgwRCqou5qNWSs130_assertion
dcterms:description
"[Polymorphisms within IL-1A influence the degree of brain microglial cell activation, especially in bearers of APOE epsilon4 allele, reinforcing the importance of neuroinflammatory processes in the pathogenesis of AD, and supporting the rationale for treating the disease with inflammation modulating drugs.]. 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:15377701
;
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:NP174508.RA7FsK4c0NxOFSyE7kKubOxKSXO6_JmkgwRCqou5qNWSs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:34+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" .
}