@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP122612.RANc5OmP9_ZW2fbWFHM--47RhAmG21Jtyz26lhCyZ245c
> .
@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/v4.0.0/void/
> .
dgn-np:NP122612.RANc5OmP9_ZW2fbWFHM--47RhAmG21Jtyz26lhCyZ245c130_head
{
this:
np:hasAssertion
dgn-np:NP122612.RANc5OmP9_ZW2fbWFHM--47RhAmG21Jtyz26lhCyZ245c130_assertion
;
np:hasProvenance
dgn-np:NP122612.RANc5OmP9_ZW2fbWFHM--47RhAmG21Jtyz26lhCyZ245c130_provenance
;
np:hasPublicationInfo
dgn-np:NP122612.RANc5OmP9_ZW2fbWFHM--47RhAmG21Jtyz26lhCyZ245c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP122612.RANc5OmP9_ZW2fbWFHM--47RhAmG21Jtyz26lhCyZ245c130_assertion
a
np:Assertion
.
dgn-np:NP122612.RANc5OmP9_ZW2fbWFHM--47RhAmG21Jtyz26lhCyZ245c130_provenance
a
np:Provenance
.
dgn-np:NP122612.RANc5OmP9_ZW2fbWFHM--47RhAmG21Jtyz26lhCyZ245c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP122612.RANc5OmP9_ZW2fbWFHM--47RhAmG21Jtyz26lhCyZ245c130_assertion
{
miriam-gene:2153
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGN77e8c15c67764264b0b41d40e2792594
sio:SIO_000628
miriam-gene:2153
,
lld:C1956346
;
a
sio:SIO_001122
.
}
dgn-np:NP122612.RANc5OmP9_ZW2fbWFHM--47RhAmG21Jtyz26lhCyZ245c130_provenance
{
dgn-np:NP122612.RANc5OmP9_ZW2fbWFHM--47RhAmG21Jtyz26lhCyZ245c130_assertion
dcterms:description
"[Although both the heterozygote Factor VLeiden and Prothrombin gene mutations were more frequent in patients with CAD than in control subjects, there was no statistical relationship found to exist between coronary artery disease and the Factor VLeiden and]. 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:18452260
;
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:NP122612.RANc5OmP9_ZW2fbWFHM--47RhAmG21Jtyz26lhCyZ245c130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:43+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}