@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP59579.RACbVFURxhnQNECEzOvFkFtUs9TS5aivAPa7R0cHRKaTE
> .
@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:NP59579.RACbVFURxhnQNECEzOvFkFtUs9TS5aivAPa7R0cHRKaTE130_head
{
this:
np:hasAssertion
dgn-np:NP59579.RACbVFURxhnQNECEzOvFkFtUs9TS5aivAPa7R0cHRKaTE130_assertion
;
np:hasProvenance
dgn-np:NP59579.RACbVFURxhnQNECEzOvFkFtUs9TS5aivAPa7R0cHRKaTE130_provenance
;
np:hasPublicationInfo
dgn-np:NP59579.RACbVFURxhnQNECEzOvFkFtUs9TS5aivAPa7R0cHRKaTE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP59579.RACbVFURxhnQNECEzOvFkFtUs9TS5aivAPa7R0cHRKaTE130_assertion
a
np:Assertion
.
dgn-np:NP59579.RACbVFURxhnQNECEzOvFkFtUs9TS5aivAPa7R0cHRKaTE130_provenance
a
np:Provenance
.
dgn-np:NP59579.RACbVFURxhnQNECEzOvFkFtUs9TS5aivAPa7R0cHRKaTE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP59579.RACbVFURxhnQNECEzOvFkFtUs9TS5aivAPa7R0cHRKaTE130_assertion
{
miriam-gene:345
a
ncit:C16612
.
lld:C0010054
a
ncit:C7057
.
dgn-gda:DGN1ef39a1508d68f1e8469f90583c228b8
sio:SIO_000628
miriam-gene:345
,
lld:C0010054
;
a
sio:SIO_001122
.
}
dgn-np:NP59579.RACbVFURxhnQNECEzOvFkFtUs9TS5aivAPa7R0cHRKaTE130_provenance
{
dgn-np:NP59579.RACbVFURxhnQNECEzOvFkFtUs9TS5aivAPa7R0cHRKaTE130_assertion
dcterms:description
"[ variation in LIPC (hepatic lipase) gene associates with clinical outcomes in Italian patients with established CAD. Further studies on the LIPC gene in CAD patients are warranted, in particular looking at the possible influences on clinical outcomes.]. 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:12964943
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP59579.RACbVFURxhnQNECEzOvFkFtUs9TS5aivAPa7R0cHRKaTE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:28+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" .
}