@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP111952.RAP9pI6lD_Cf1-TNb7imwG6qf5xh9OvWR_8tepvMyg_tk
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP111952.RAP9pI6lD_Cf1-TNb7imwG6qf5xh9OvWR_8tepvMyg_tk130_head
{
this:
np:hasAssertion
dgn-np:NP111952.RAP9pI6lD_Cf1-TNb7imwG6qf5xh9OvWR_8tepvMyg_tk130_assertion
;
np:hasProvenance
dgn-np:NP111952.RAP9pI6lD_Cf1-TNb7imwG6qf5xh9OvWR_8tepvMyg_tk130_provenance
;
np:hasPublicationInfo
dgn-np:NP111952.RAP9pI6lD_Cf1-TNb7imwG6qf5xh9OvWR_8tepvMyg_tk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP111952.RAP9pI6lD_Cf1-TNb7imwG6qf5xh9OvWR_8tepvMyg_tk130_assertion
a
np:Assertion
.
dgn-np:NP111952.RAP9pI6lD_Cf1-TNb7imwG6qf5xh9OvWR_8tepvMyg_tk130_provenance
a
np:Provenance
.
dgn-np:NP111952.RAP9pI6lD_Cf1-TNb7imwG6qf5xh9OvWR_8tepvMyg_tk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP111952.RAP9pI6lD_Cf1-TNb7imwG6qf5xh9OvWR_8tepvMyg_tk130_assertion
{
miriam-gene:1557
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGNf4f31fca82c4d1d7e7ba8f9cf070636b
sio:SIO_000628
miriam-gene:1557
,
lld:C0007222
;
a
sio:SIO_001122
.
}
dgn-np:NP111952.RAP9pI6lD_Cf1-TNb7imwG6qf5xh9OvWR_8tepvMyg_tk130_provenance
{
dgn-np:NP111952.RAP9pI6lD_Cf1-TNb7imwG6qf5xh9OvWR_8tepvMyg_tk130_assertion
dcterms:description
"[Individuals with the ABCB1 3435 TT genotype have reduced platelet inhibition and are at increased risk of recurrent ischaemic events during clopidogrel treatment. In patients with acute coronary syndromes who have undergone percutaneous intervention, when]. 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:20801494
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP111952.RAP9pI6lD_Cf1-TNb7imwG6qf5xh9OvWR_8tepvMyg_tk130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:42+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}