@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP254832.RABnk_i3aQpyjg9BrgIfRkgBOD8PKxCsulzt98NY01vNA
> .
@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:NP254832.RABnk_i3aQpyjg9BrgIfRkgBOD8PKxCsulzt98NY01vNA130_head
{
this:
np:hasAssertion
dgn-np:NP254832.RABnk_i3aQpyjg9BrgIfRkgBOD8PKxCsulzt98NY01vNA130_assertion
;
np:hasProvenance
dgn-np:NP254832.RABnk_i3aQpyjg9BrgIfRkgBOD8PKxCsulzt98NY01vNA130_provenance
;
np:hasPublicationInfo
dgn-np:NP254832.RABnk_i3aQpyjg9BrgIfRkgBOD8PKxCsulzt98NY01vNA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP254832.RABnk_i3aQpyjg9BrgIfRkgBOD8PKxCsulzt98NY01vNA130_assertion
a
np:Assertion
.
dgn-np:NP254832.RABnk_i3aQpyjg9BrgIfRkgBOD8PKxCsulzt98NY01vNA130_provenance
a
np:Provenance
.
dgn-np:NP254832.RABnk_i3aQpyjg9BrgIfRkgBOD8PKxCsulzt98NY01vNA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP254832.RABnk_i3aQpyjg9BrgIfRkgBOD8PKxCsulzt98NY01vNA130_assertion
{
miriam-gene:19
a
ncit:C16612
.
lld:C0004153
a
ncit:C7057
.
dgn-gda:DGN70d46ef0abe130e88b7e0d53b2f496fd
sio:SIO_000628
miriam-gene:19
,
lld:C0004153
;
a
sio:SIO_001121
.
}
dgn-np:NP254832.RABnk_i3aQpyjg9BrgIfRkgBOD8PKxCsulzt98NY01vNA130_provenance
{
dgn-np:NP254832.RABnk_i3aQpyjg9BrgIfRkgBOD8PKxCsulzt98NY01vNA130_assertion
dcterms:description
"[Carotid intima-media thickness (cIMT) measurements were obtained in cases comprising 10 different mutations in LCAT, ABCA1 and APOA1 to further evaluate the relationship between low HDL resulting from genetic variation and early atherosclerosis.]. 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:17113061
;
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:NP254832.RABnk_i3aQpyjg9BrgIfRkgBOD8PKxCsulzt98NY01vNA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:22+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" .
}