@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP812667.RAVRsiYqjUuVCNA5oBJEHnO_Vj9Bxh7_pE-M3kOQNgAnw
> .
@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:NP812667.RAVRsiYqjUuVCNA5oBJEHnO_Vj9Bxh7_pE-M3kOQNgAnw130_head
{
this:
np:hasAssertion
dgn-np:NP812667.RAVRsiYqjUuVCNA5oBJEHnO_Vj9Bxh7_pE-M3kOQNgAnw130_assertion
;
np:hasProvenance
dgn-np:NP812667.RAVRsiYqjUuVCNA5oBJEHnO_Vj9Bxh7_pE-M3kOQNgAnw130_provenance
;
np:hasPublicationInfo
dgn-np:NP812667.RAVRsiYqjUuVCNA5oBJEHnO_Vj9Bxh7_pE-M3kOQNgAnw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP812667.RAVRsiYqjUuVCNA5oBJEHnO_Vj9Bxh7_pE-M3kOQNgAnw130_assertion
a
np:Assertion
.
dgn-np:NP812667.RAVRsiYqjUuVCNA5oBJEHnO_Vj9Bxh7_pE-M3kOQNgAnw130_provenance
a
np:Provenance
.
dgn-np:NP812667.RAVRsiYqjUuVCNA5oBJEHnO_Vj9Bxh7_pE-M3kOQNgAnw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP812667.RAVRsiYqjUuVCNA5oBJEHnO_Vj9Bxh7_pE-M3kOQNgAnw130_assertion
{
miriam-gene:6403
a
ncit:C16612
.
lld:C0020443
a
ncit:C7057
.
dgn-gda:DGNf38309470689467c1cc162c04d3df6ea
sio:SIO_000628
miriam-gene:6403
,
lld:C0020443
;
a
sio:SIO_001121
.
}
dgn-np:NP812667.RAVRsiYqjUuVCNA5oBJEHnO_Vj9Bxh7_pE-M3kOQNgAnw130_provenance
{
dgn-np:NP812667.RAVRsiYqjUuVCNA5oBJEHnO_Vj9Bxh7_pE-M3kOQNgAnw130_assertion
dcterms:description
"[There was no significant association between conventional risk factors (such as hypercholesterolaemia, increased body mass index, or raised blood pressure) and either the rare or the common Pro(715) allele of the P-selectin gene in controls.]. 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:11040019
;
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:NP812667.RAVRsiYqjUuVCNA5oBJEHnO_Vj9Bxh7_pE-M3kOQNgAnw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:18+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" .
}