@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP878607.RAM29nCqEMHA5cBAdX5mRlxh38xcqPl9QNcX1c943Ze2M
> .
@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:NP878607.RAM29nCqEMHA5cBAdX5mRlxh38xcqPl9QNcX1c943Ze2M130_head
{
this:
np:hasAssertion
dgn-np:NP878607.RAM29nCqEMHA5cBAdX5mRlxh38xcqPl9QNcX1c943Ze2M130_assertion
;
np:hasProvenance
dgn-np:NP878607.RAM29nCqEMHA5cBAdX5mRlxh38xcqPl9QNcX1c943Ze2M130_provenance
;
np:hasPublicationInfo
dgn-np:NP878607.RAM29nCqEMHA5cBAdX5mRlxh38xcqPl9QNcX1c943Ze2M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP878607.RAM29nCqEMHA5cBAdX5mRlxh38xcqPl9QNcX1c943Ze2M130_assertion
a
np:Assertion
.
dgn-np:NP878607.RAM29nCqEMHA5cBAdX5mRlxh38xcqPl9QNcX1c943Ze2M130_provenance
a
np:Provenance
.
dgn-np:NP878607.RAM29nCqEMHA5cBAdX5mRlxh38xcqPl9QNcX1c943Ze2M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP878607.RAM29nCqEMHA5cBAdX5mRlxh38xcqPl9QNcX1c943Ze2M130_assertion
{
miriam-gene:6584
a
ncit:C16612
.
lld:C3463824
a
ncit:C7057
.
dgn-gda:DGNaf43aecb0b2d4d9f3aae2111b70e2eea
sio:SIO_000628
miriam-gene:6584
,
lld:C3463824
;
a
sio:SIO_001121
.
}
dgn-np:NP878607.RAM29nCqEMHA5cBAdX5mRlxh38xcqPl9QNcX1c943Ze2M130_provenance
{
dgn-np:NP878607.RAM29nCqEMHA5cBAdX5mRlxh38xcqPl9QNcX1c943Ze2M130_assertion
dcterms:description
"[Considering the risk of acquiring a myelodysplastic syndrome (MDS) with age, the aim of this study was to quantify mRNA synthesis of the carnitine palmitoyltransferases (CPT1 and CPT2), carnitine acetyltransferase (CRAT), human specific microsomal CPT, and OCTN2 (organic cation transporter) in mononuclear cells of healthy humans of different age groups and MDS patients.]. 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:12802501
;
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:NP878607.RAM29nCqEMHA5cBAdX5mRlxh38xcqPl9QNcX1c943Ze2M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:57+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" .
}