@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP200265.RASXClYDz_Wkzsjjvlkko_FEL9N6jYbuBEsJASCZaDor0
> .
@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:NP200265.RASXClYDz_Wkzsjjvlkko_FEL9N6jYbuBEsJASCZaDor0130_head
{
this:
np:hasAssertion
dgn-np:NP200265.RASXClYDz_Wkzsjjvlkko_FEL9N6jYbuBEsJASCZaDor0130_assertion
;
np:hasProvenance
dgn-np:NP200265.RASXClYDz_Wkzsjjvlkko_FEL9N6jYbuBEsJASCZaDor0130_provenance
;
np:hasPublicationInfo
dgn-np:NP200265.RASXClYDz_Wkzsjjvlkko_FEL9N6jYbuBEsJASCZaDor0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP200265.RASXClYDz_Wkzsjjvlkko_FEL9N6jYbuBEsJASCZaDor0130_assertion
a
np:Assertion
.
dgn-np:NP200265.RASXClYDz_Wkzsjjvlkko_FEL9N6jYbuBEsJASCZaDor0130_provenance
a
np:Provenance
.
dgn-np:NP200265.RASXClYDz_Wkzsjjvlkko_FEL9N6jYbuBEsJASCZaDor0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP200265.RASXClYDz_Wkzsjjvlkko_FEL9N6jYbuBEsJASCZaDor0130_assertion
{
miriam-gene:1071
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGNd9e8e883aa861ebc556895439a6e6f64
sio:SIO_000628
miriam-gene:1071
,
lld:C1956346
;
a
sio:SIO_001121
.
}
dgn-np:NP200265.RASXClYDz_Wkzsjjvlkko_FEL9N6jYbuBEsJASCZaDor0130_provenance
{
dgn-np:NP200265.RASXClYDz_Wkzsjjvlkko_FEL9N6jYbuBEsJASCZaDor0130_assertion
dcterms:description
"[The study thus indicated that genetic variation of APOB, LPL, CETP, and lecithin cholesterol acyl transferase (which is linked to HPA and CETP) may play an important role in the regulation of lipoprotein metabolism and could contribute to the risk of coronary artery disease.]. 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:8279486
;
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:NP200265.RASXClYDz_Wkzsjjvlkko_FEL9N6jYbuBEsJASCZaDor0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:50+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" .
}