@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP468776.RA3spF6Fcz5uFIeUYipQ7-8_x9hoccWDUXAI7q3H441Bw
> .
@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:NP468776.RA3spF6Fcz5uFIeUYipQ7-8_x9hoccWDUXAI7q3H441Bw130_head
{
this:
np:hasAssertion
dgn-np:NP468776.RA3spF6Fcz5uFIeUYipQ7-8_x9hoccWDUXAI7q3H441Bw130_assertion
;
np:hasProvenance
dgn-np:NP468776.RA3spF6Fcz5uFIeUYipQ7-8_x9hoccWDUXAI7q3H441Bw130_provenance
;
np:hasPublicationInfo
dgn-np:NP468776.RA3spF6Fcz5uFIeUYipQ7-8_x9hoccWDUXAI7q3H441Bw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP468776.RA3spF6Fcz5uFIeUYipQ7-8_x9hoccWDUXAI7q3H441Bw130_assertion
a
np:Assertion
.
dgn-np:NP468776.RA3spF6Fcz5uFIeUYipQ7-8_x9hoccWDUXAI7q3H441Bw130_provenance
a
np:Provenance
.
dgn-np:NP468776.RA3spF6Fcz5uFIeUYipQ7-8_x9hoccWDUXAI7q3H441Bw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP468776.RA3spF6Fcz5uFIeUYipQ7-8_x9hoccWDUXAI7q3H441Bw130_assertion
{
miriam-gene:2169
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGN6655cc60ae2ca4abc3d7f5fe37a5472f
sio:SIO_000628
miriam-gene:2169
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP468776.RA3spF6Fcz5uFIeUYipQ7-8_x9hoccWDUXAI7q3H441Bw130_provenance
{
dgn-np:NP468776.RA3spF6Fcz5uFIeUYipQ7-8_x9hoccWDUXAI7q3H441Bw130_assertion
dcterms:description
"[Our aim was to investigate the frequency of the alanine (Ala) 54Thr polymorphism of the FABP2 gene in patients with coronary heart disease (CHD), and the association between the polymorphism and the markers of metabolic syndrome, serum lipid levels and the fatty acid profile of serum lipids.]. 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:12189904
;
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:NP468776.RA3spF6Fcz5uFIeUYipQ7-8_x9hoccWDUXAI7q3H441Bw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:41+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" .
}