@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP511511.RAq9aOL7D9KOVBWaZ93yvbablG_nQ3YHMeWwxdsbP4tvk
> .
@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:NP511511.RAq9aOL7D9KOVBWaZ93yvbablG_nQ3YHMeWwxdsbP4tvk130_head
{
this:
np:hasAssertion
dgn-np:NP511511.RAq9aOL7D9KOVBWaZ93yvbablG_nQ3YHMeWwxdsbP4tvk130_assertion
;
np:hasProvenance
dgn-np:NP511511.RAq9aOL7D9KOVBWaZ93yvbablG_nQ3YHMeWwxdsbP4tvk130_provenance
;
np:hasPublicationInfo
dgn-np:NP511511.RAq9aOL7D9KOVBWaZ93yvbablG_nQ3YHMeWwxdsbP4tvk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP511511.RAq9aOL7D9KOVBWaZ93yvbablG_nQ3YHMeWwxdsbP4tvk130_assertion
a
np:Assertion
.
dgn-np:NP511511.RAq9aOL7D9KOVBWaZ93yvbablG_nQ3YHMeWwxdsbP4tvk130_provenance
a
np:Provenance
.
dgn-np:NP511511.RAq9aOL7D9KOVBWaZ93yvbablG_nQ3YHMeWwxdsbP4tvk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP511511.RAq9aOL7D9KOVBWaZ93yvbablG_nQ3YHMeWwxdsbP4tvk130_assertion
{
miriam-gene:5555
a
ncit:C16612
.
lld:C0038454
a
ncit:C7057
.
dgn-gda:DGNfa0a233cd331be30fb22430d1bbc4db9
sio:SIO_000628
miriam-gene:5555
,
lld:C0038454
;
a
sio:SIO_001121
.
}
dgn-np:NP511511.RAq9aOL7D9KOVBWaZ93yvbablG_nQ3YHMeWwxdsbP4tvk130_provenance
{
dgn-np:NP511511.RAq9aOL7D9KOVBWaZ93yvbablG_nQ3YHMeWwxdsbP4tvk130_assertion
dcterms:description
"[We assessed the occurrence of several prothrombotic states (factor V Leiden, prothrombin G20210A, deficiencies in protein S, protein C and antithrombin, lupus anticoagulant, anticardiolipin antibodies, elevated factor VIII, resistance to activated protein C) and classical risk factors for venous thrombosis in 57 adult patients with cryptogenic stroke and patent foramen ovale and in 104 matched 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:12695749
;
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:NP511511.RAq9aOL7D9KOVBWaZ93yvbablG_nQ3YHMeWwxdsbP4tvk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:05+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" .
}