@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP540128.RAzu1KI1YMwsyd4T4McDbtqYZkLg0OvqBPbdv9vIc96bY
> .
@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:NP540128.RAzu1KI1YMwsyd4T4McDbtqYZkLg0OvqBPbdv9vIc96bY130_head
{
this:
np:hasAssertion
dgn-np:NP540128.RAzu1KI1YMwsyd4T4McDbtqYZkLg0OvqBPbdv9vIc96bY130_assertion
;
np:hasProvenance
dgn-np:NP540128.RAzu1KI1YMwsyd4T4McDbtqYZkLg0OvqBPbdv9vIc96bY130_provenance
;
np:hasPublicationInfo
dgn-np:NP540128.RAzu1KI1YMwsyd4T4McDbtqYZkLg0OvqBPbdv9vIc96bY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP540128.RAzu1KI1YMwsyd4T4McDbtqYZkLg0OvqBPbdv9vIc96bY130_assertion
a
np:Assertion
.
dgn-np:NP540128.RAzu1KI1YMwsyd4T4McDbtqYZkLg0OvqBPbdv9vIc96bY130_provenance
a
np:Provenance
.
dgn-np:NP540128.RAzu1KI1YMwsyd4T4McDbtqYZkLg0OvqBPbdv9vIc96bY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP540128.RAzu1KI1YMwsyd4T4McDbtqYZkLg0OvqBPbdv9vIc96bY130_assertion
{
miriam-gene:6401
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGNd5b7caa3535729b23999fdc3b215a9eb
sio:SIO_000628
miriam-gene:6401
,
lld:C1956346
;
a
sio:SIO_001121
.
}
dgn-np:NP540128.RAzu1KI1YMwsyd4T4McDbtqYZkLg0OvqBPbdv9vIc96bY130_provenance
{
dgn-np:NP540128.RAzu1KI1YMwsyd4T4McDbtqYZkLg0OvqBPbdv9vIc96bY130_assertion
dcterms:description
"[The E-selectin p. S128R (g. A561C) polymorphism has been associated with the presence of angiographic coronary artery disease (CAD) in some populations, but no data is currently available on its association with CAD in Arabs.]. 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:16756647
;
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:NP540128.RAzu1KI1YMwsyd4T4McDbtqYZkLg0OvqBPbdv9vIc96bY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:25+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" .
}