@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP433232.RAZyGHCkY-Y0-mKH-r3SnGRRNTBSlelw1SvBxW4Nd_i58
> .
@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:NP433232.RAZyGHCkY-Y0-mKH-r3SnGRRNTBSlelw1SvBxW4Nd_i58130_head
{
this:
np:hasAssertion
dgn-np:NP433232.RAZyGHCkY-Y0-mKH-r3SnGRRNTBSlelw1SvBxW4Nd_i58130_assertion
;
np:hasProvenance
dgn-np:NP433232.RAZyGHCkY-Y0-mKH-r3SnGRRNTBSlelw1SvBxW4Nd_i58130_provenance
;
np:hasPublicationInfo
dgn-np:NP433232.RAZyGHCkY-Y0-mKH-r3SnGRRNTBSlelw1SvBxW4Nd_i58130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP433232.RAZyGHCkY-Y0-mKH-r3SnGRRNTBSlelw1SvBxW4Nd_i58130_assertion
a
np:Assertion
.
dgn-np:NP433232.RAZyGHCkY-Y0-mKH-r3SnGRRNTBSlelw1SvBxW4Nd_i58130_provenance
a
np:Provenance
.
dgn-np:NP433232.RAZyGHCkY-Y0-mKH-r3SnGRRNTBSlelw1SvBxW4Nd_i58130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP433232.RAZyGHCkY-Y0-mKH-r3SnGRRNTBSlelw1SvBxW4Nd_i58130_assertion
{
miriam-gene:2153
a
ncit:C16612
.
lld:C0340708
a
ncit:C7057
.
dgn-gda:DGN04de9f9b8e0fb38e3f9ad874b293a2e4
sio:SIO_000628
miriam-gene:2153
,
lld:C0340708
;
a
sio:SIO_001121
.
}
dgn-np:NP433232.RAZyGHCkY-Y0-mKH-r3SnGRRNTBSlelw1SvBxW4Nd_i58130_provenance
{
dgn-np:NP433232.RAZyGHCkY-Y0-mKH-r3SnGRRNTBSlelw1SvBxW4Nd_i58130_assertion
dcterms:description
"[Association of a mutation in the coagulation factor V gene (FV Leiden) with deep vein thrombosis and pulmonary thromboembolism has been well documented in the literature, but no study has specifically screened cases of fatal pulmonary thromboembolism for the mutation.]. 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:9700847
;
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:NP433232.RAZyGHCkY-Y0-mKH-r3SnGRRNTBSlelw1SvBxW4Nd_i58130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:16+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" .
}