@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP836300.RAYQXxIC_jzTzo_bnMjuYyodgLrZ6GYlwwfBkhYDVQpXc
> .
@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:NP836300.RAYQXxIC_jzTzo_bnMjuYyodgLrZ6GYlwwfBkhYDVQpXc130_head
{
this:
np:hasAssertion
dgn-np:NP836300.RAYQXxIC_jzTzo_bnMjuYyodgLrZ6GYlwwfBkhYDVQpXc130_assertion
;
np:hasProvenance
dgn-np:NP836300.RAYQXxIC_jzTzo_bnMjuYyodgLrZ6GYlwwfBkhYDVQpXc130_provenance
;
np:hasPublicationInfo
dgn-np:NP836300.RAYQXxIC_jzTzo_bnMjuYyodgLrZ6GYlwwfBkhYDVQpXc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP836300.RAYQXxIC_jzTzo_bnMjuYyodgLrZ6GYlwwfBkhYDVQpXc130_assertion
a
np:Assertion
.
dgn-np:NP836300.RAYQXxIC_jzTzo_bnMjuYyodgLrZ6GYlwwfBkhYDVQpXc130_provenance
a
np:Provenance
.
dgn-np:NP836300.RAYQXxIC_jzTzo_bnMjuYyodgLrZ6GYlwwfBkhYDVQpXc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP836300.RAYQXxIC_jzTzo_bnMjuYyodgLrZ6GYlwwfBkhYDVQpXc130_assertion
{
miriam-gene:19
a
ncit:C16612
.
lld:C3272363
a
ncit:C7057
.
dgn-gda:DGNd047116584d4ac4d16a4cf1da078b0b8
sio:SIO_000628
miriam-gene:19
,
lld:C3272363
;
a
sio:SIO_001121
.
}
dgn-np:NP836300.RAYQXxIC_jzTzo_bnMjuYyodgLrZ6GYlwwfBkhYDVQpXc130_provenance
{
dgn-np:NP836300.RAYQXxIC_jzTzo_bnMjuYyodgLrZ6GYlwwfBkhYDVQpXc130_assertion
dcterms:description
"[We investigated 244 unrelated, consecutively enrolled patients with ischemic stroke, 150 patients with coronary heart disease (CHD) and 193 blood donors for allele frequencies (AFs) of three common ABCA1 polymorphisms (R219K, V771M and I883M).]. 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:16446539
;
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:NP836300.RAYQXxIC_jzTzo_bnMjuYyodgLrZ6GYlwwfBkhYDVQpXc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:31+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" .
}