@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP130182.RAmNVqMqHJU_p9FFbPhBIZn2CFDW1iZZx0ZTj1Fo1Pmuk
> .
@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:NP130182.RAmNVqMqHJU_p9FFbPhBIZn2CFDW1iZZx0ZTj1Fo1Pmuk130_head
{
this:
np:hasAssertion
dgn-np:NP130182.RAmNVqMqHJU_p9FFbPhBIZn2CFDW1iZZx0ZTj1Fo1Pmuk130_assertion
;
np:hasProvenance
dgn-np:NP130182.RAmNVqMqHJU_p9FFbPhBIZn2CFDW1iZZx0ZTj1Fo1Pmuk130_provenance
;
np:hasPublicationInfo
dgn-np:NP130182.RAmNVqMqHJU_p9FFbPhBIZn2CFDW1iZZx0ZTj1Fo1Pmuk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP130182.RAmNVqMqHJU_p9FFbPhBIZn2CFDW1iZZx0ZTj1Fo1Pmuk130_assertion
a
np:Assertion
.
dgn-np:NP130182.RAmNVqMqHJU_p9FFbPhBIZn2CFDW1iZZx0ZTj1Fo1Pmuk130_provenance
a
np:Provenance
.
dgn-np:NP130182.RAmNVqMqHJU_p9FFbPhBIZn2CFDW1iZZx0ZTj1Fo1Pmuk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP130182.RAmNVqMqHJU_p9FFbPhBIZn2CFDW1iZZx0ZTj1Fo1Pmuk130_assertion
{
miriam-gene:4332
a
ncit:C16612
.
lld:C0004153
a
ncit:C7057
.
dgn-gda:DGN2dbf92aa0cb4bddb25c21dc3fbd5fb41
sio:SIO_000628
miriam-gene:4332
,
lld:C0004153
;
a
sio:SIO_001122
.
}
dgn-np:NP130182.RAmNVqMqHJU_p9FFbPhBIZn2CFDW1iZZx0ZTj1Fo1Pmuk130_provenance
{
dgn-np:NP130182.RAmNVqMqHJU_p9FFbPhBIZn2CFDW1iZZx0ZTj1Fo1Pmuk130_assertion
dcterms:description
"[variation in MNDA expression appeared to change with phenotypic specialization of monocytes in atherosclerosis consistent with its association with inflammation and suspected roles in regulating gene expression or in mediating cell death ]. 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:15778972
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP130182.RAmNVqMqHJU_p9FFbPhBIZn2CFDW1iZZx0ZTj1Fo1Pmuk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:07+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" .
}