@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP49458.RAhNEJfnV8Kaoy-v2pKJnQQ0RXf8fkueg7pnxqpUVNmS4
> .
@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:NP49458.RAhNEJfnV8Kaoy-v2pKJnQQ0RXf8fkueg7pnxqpUVNmS4130_head
{
this:
np:hasAssertion
dgn-np:NP49458.RAhNEJfnV8Kaoy-v2pKJnQQ0RXf8fkueg7pnxqpUVNmS4130_assertion
;
np:hasProvenance
dgn-np:NP49458.RAhNEJfnV8Kaoy-v2pKJnQQ0RXf8fkueg7pnxqpUVNmS4130_provenance
;
np:hasPublicationInfo
dgn-np:NP49458.RAhNEJfnV8Kaoy-v2pKJnQQ0RXf8fkueg7pnxqpUVNmS4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP49458.RAhNEJfnV8Kaoy-v2pKJnQQ0RXf8fkueg7pnxqpUVNmS4130_assertion
a
np:Assertion
.
dgn-np:NP49458.RAhNEJfnV8Kaoy-v2pKJnQQ0RXf8fkueg7pnxqpUVNmS4130_provenance
a
np:Provenance
.
dgn-np:NP49458.RAhNEJfnV8Kaoy-v2pKJnQQ0RXf8fkueg7pnxqpUVNmS4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP49458.RAhNEJfnV8Kaoy-v2pKJnQQ0RXf8fkueg7pnxqpUVNmS4130_assertion
{
miriam-gene:1636
a
ncit:C16612
.
lld:C0333186
a
ncit:C7057
.
dgn-gda:DGNf93b457e862d51e5ae65e18171c4b706
sio:SIO_000628
miriam-gene:1636
,
lld:C0333186
;
a
sio:SIO_001122
.
}
dgn-np:NP49458.RAhNEJfnV8Kaoy-v2pKJnQQ0RXf8fkueg7pnxqpUVNmS4130_provenance
{
dgn-np:NP49458.RAhNEJfnV8Kaoy-v2pKJnQQ0RXf8fkueg7pnxqpUVNmS4130_assertion
dcterms:description
"[Thus, knowledge of the haptoglobin phenotype may be useful in assessing and utilizing new therapies that attempt to reduce restenosis, and may have important implications for the risk stratification algorithm used in managing diabetic patients with 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:11909563
;
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:NP49458.RAhNEJfnV8Kaoy-v2pKJnQQ0RXf8fkueg7pnxqpUVNmS4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}