@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP496148.RAq76glCNl7Zn63PU0eRfaJFM5nXBoldE7-XkPVrnjGhA
> .
@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:NP496148.RAq76glCNl7Zn63PU0eRfaJFM5nXBoldE7-XkPVrnjGhA130_head
{
this:
np:hasAssertion
dgn-np:NP496148.RAq76glCNl7Zn63PU0eRfaJFM5nXBoldE7-XkPVrnjGhA130_assertion
;
np:hasProvenance
dgn-np:NP496148.RAq76glCNl7Zn63PU0eRfaJFM5nXBoldE7-XkPVrnjGhA130_provenance
;
np:hasPublicationInfo
dgn-np:NP496148.RAq76glCNl7Zn63PU0eRfaJFM5nXBoldE7-XkPVrnjGhA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP496148.RAq76glCNl7Zn63PU0eRfaJFM5nXBoldE7-XkPVrnjGhA130_assertion
a
np:Assertion
.
dgn-np:NP496148.RAq76glCNl7Zn63PU0eRfaJFM5nXBoldE7-XkPVrnjGhA130_provenance
a
np:Provenance
.
dgn-np:NP496148.RAq76glCNl7Zn63PU0eRfaJFM5nXBoldE7-XkPVrnjGhA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP496148.RAq76glCNl7Zn63PU0eRfaJFM5nXBoldE7-XkPVrnjGhA130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C1861171
a
ncit:C7057
.
dgn-gda:DGN21e555e38ffb0de13cae238b731811ba
sio:SIO_000628
miriam-gene:4524
,
lld:C1861171
;
a
sio:SIO_001121
.
}
dgn-np:NP496148.RAq76glCNl7Zn63PU0eRfaJFM5nXBoldE7-XkPVrnjGhA130_provenance
{
dgn-np:NP496148.RAq76glCNl7Zn63PU0eRfaJFM5nXBoldE7-XkPVrnjGhA130_assertion
dcterms:description
"[Activated protein C resistance due to factor V Leiden heterozygous and heterozygocity for the methylenetetrahydrofolate reductase were diagnosed and suspected to be the risk factors that contribute to the development of the deep vein thrombosis in this SCA patient.]. 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:10505325
;
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:NP496148.RAq76glCNl7Zn63PU0eRfaJFM5nXBoldE7-XkPVrnjGhA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:56+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" .
}