@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP792392.RAnZ0pfrw4GxAtKtUop1SNeFsKecyzy9zTWcnaTcoTmDE
> .
@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:NP792392.RAnZ0pfrw4GxAtKtUop1SNeFsKecyzy9zTWcnaTcoTmDE130_head
{
this:
np:hasAssertion
dgn-np:NP792392.RAnZ0pfrw4GxAtKtUop1SNeFsKecyzy9zTWcnaTcoTmDE130_assertion
;
np:hasProvenance
dgn-np:NP792392.RAnZ0pfrw4GxAtKtUop1SNeFsKecyzy9zTWcnaTcoTmDE130_provenance
;
np:hasPublicationInfo
dgn-np:NP792392.RAnZ0pfrw4GxAtKtUop1SNeFsKecyzy9zTWcnaTcoTmDE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP792392.RAnZ0pfrw4GxAtKtUop1SNeFsKecyzy9zTWcnaTcoTmDE130_assertion
a
np:Assertion
.
dgn-np:NP792392.RAnZ0pfrw4GxAtKtUop1SNeFsKecyzy9zTWcnaTcoTmDE130_provenance
a
np:Provenance
.
dgn-np:NP792392.RAnZ0pfrw4GxAtKtUop1SNeFsKecyzy9zTWcnaTcoTmDE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP792392.RAnZ0pfrw4GxAtKtUop1SNeFsKecyzy9zTWcnaTcoTmDE130_assertion
{
miriam-gene:1071
a
ncit:C16612
.
lld:C0334121
a
ncit:C7057
.
dgn-gda:DGN73605254bd9bb5acdfcb9bcb3e73b633
sio:SIO_000628
miriam-gene:1071
,
lld:C0334121
;
a
sio:SIO_001121
.
}
dgn-np:NP792392.RAnZ0pfrw4GxAtKtUop1SNeFsKecyzy9zTWcnaTcoTmDE130_provenance
{
dgn-np:NP792392.RAnZ0pfrw4GxAtKtUop1SNeFsKecyzy9zTWcnaTcoTmDE130_assertion
dcterms:description
"[Some researchers have reported that IMT is high in people with functional variants of genes related to matrix deposition (MMP3), inflammation (interleukin 6), and lipid metabolism (hepatic lipase, APOE, CETP, and PON1).]. 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:15039035
;
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:NP792392.RAnZ0pfrw4GxAtKtUop1SNeFsKecyzy9zTWcnaTcoTmDE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:06+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" .
}