@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP587268.RAkwyeUg3hSG_v1-Bf5bBtvgeQkhvUxXylO57WGvyDRRI
> .
@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:NP587268.RAkwyeUg3hSG_v1-Bf5bBtvgeQkhvUxXylO57WGvyDRRI130_head
{
this:
np:hasAssertion
dgn-np:NP587268.RAkwyeUg3hSG_v1-Bf5bBtvgeQkhvUxXylO57WGvyDRRI130_assertion
;
np:hasProvenance
dgn-np:NP587268.RAkwyeUg3hSG_v1-Bf5bBtvgeQkhvUxXylO57WGvyDRRI130_provenance
;
np:hasPublicationInfo
dgn-np:NP587268.RAkwyeUg3hSG_v1-Bf5bBtvgeQkhvUxXylO57WGvyDRRI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP587268.RAkwyeUg3hSG_v1-Bf5bBtvgeQkhvUxXylO57WGvyDRRI130_assertion
a
np:Assertion
.
dgn-np:NP587268.RAkwyeUg3hSG_v1-Bf5bBtvgeQkhvUxXylO57WGvyDRRI130_provenance
a
np:Provenance
.
dgn-np:NP587268.RAkwyeUg3hSG_v1-Bf5bBtvgeQkhvUxXylO57WGvyDRRI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP587268.RAkwyeUg3hSG_v1-Bf5bBtvgeQkhvUxXylO57WGvyDRRI130_assertion
{
miriam-gene:2212
a
ncit:C16612
.
lld:C0175697
a
ncit:C7057
.
dgn-gda:DGN08738fa6b2cfdbdbfe2174831f82131f
sio:SIO_000628
miriam-gene:2212
,
lld:C0175697
;
a
sio:SIO_001121
.
}
dgn-np:NP587268.RAkwyeUg3hSG_v1-Bf5bBtvgeQkhvUxXylO57WGvyDRRI130_provenance
{
dgn-np:NP587268.RAkwyeUg3hSG_v1-Bf5bBtvgeQkhvUxXylO57WGvyDRRI130_assertion
dcterms:description
"[While the majority of LPS-induced changes were not modulated by either statin, few select genes responded differently after statin treatment, such as the genes encoding the CD32 receptor (FCGR2A) or the protein geranylgeranyltransferase 1b subunit (PGGT1B).]. 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:18192897
;
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:NP587268.RAkwyeUg3hSG_v1-Bf5bBtvgeQkhvUxXylO57WGvyDRRI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:53+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" .
}