@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP216453.RA-Rg_2ukIHnIDDimoA7kUbjrOWdUt_clzQ1xUOu0_ctM
> .
@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:NP216453.RA-Rg_2ukIHnIDDimoA7kUbjrOWdUt_clzQ1xUOu0_ctM130_head
{
this:
np:hasAssertion
dgn-np:NP216453.RA-Rg_2ukIHnIDDimoA7kUbjrOWdUt_clzQ1xUOu0_ctM130_assertion
;
np:hasProvenance
dgn-np:NP216453.RA-Rg_2ukIHnIDDimoA7kUbjrOWdUt_clzQ1xUOu0_ctM130_provenance
;
np:hasPublicationInfo
dgn-np:NP216453.RA-Rg_2ukIHnIDDimoA7kUbjrOWdUt_clzQ1xUOu0_ctM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP216453.RA-Rg_2ukIHnIDDimoA7kUbjrOWdUt_clzQ1xUOu0_ctM130_assertion
a
np:Assertion
.
dgn-np:NP216453.RA-Rg_2ukIHnIDDimoA7kUbjrOWdUt_clzQ1xUOu0_ctM130_provenance
a
np:Provenance
.
dgn-np:NP216453.RA-Rg_2ukIHnIDDimoA7kUbjrOWdUt_clzQ1xUOu0_ctM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP216453.RA-Rg_2ukIHnIDDimoA7kUbjrOWdUt_clzQ1xUOu0_ctM130_assertion
{
miriam-gene:2153
a
ncit:C16612
.
lld:C0398623
a
ncit:C7057
.
dgn-gda:DGN4bc8a14dd93e9ce20932009554d6589e
sio:SIO_000628
miriam-gene:2153
,
lld:C0398623
;
a
sio:SIO_001121
.
}
dgn-np:NP216453.RA-Rg_2ukIHnIDDimoA7kUbjrOWdUt_clzQ1xUOu0_ctM130_provenance
{
dgn-np:NP216453.RA-Rg_2ukIHnIDDimoA7kUbjrOWdUt_clzQ1xUOu0_ctM130_assertion
dcterms:description
"[The purpose of our work was to reveal the frequency of FVL in Slovak patients with venous thromboses, to characterise the nature of venous thromboses in this inherited thrombophilia, and to consider the screening approach to investigation of FVL in patients with venous thromboses.]. 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:15815078
;
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:NP216453.RA-Rg_2ukIHnIDDimoA7kUbjrOWdUt_clzQ1xUOu0_ctM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:00+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" .
}