@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP107937.RAksOZxMlMmHkMVMnPV9RXXFmNw6SyaeNnVEGmVFRRSd4
> .
@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/v3.0.0/void/
> .
dgn-np:NP107937.RAksOZxMlMmHkMVMnPV9RXXFmNw6SyaeNnVEGmVFRRSd4130_head
{
this:
np:hasAssertion
dgn-np:NP107937.RAksOZxMlMmHkMVMnPV9RXXFmNw6SyaeNnVEGmVFRRSd4130_assertion
;
np:hasProvenance
dgn-np:NP107937.RAksOZxMlMmHkMVMnPV9RXXFmNw6SyaeNnVEGmVFRRSd4130_provenance
;
np:hasPublicationInfo
dgn-np:NP107937.RAksOZxMlMmHkMVMnPV9RXXFmNw6SyaeNnVEGmVFRRSd4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP107937.RAksOZxMlMmHkMVMnPV9RXXFmNw6SyaeNnVEGmVFRRSd4130_assertion
a
np:Assertion
.
dgn-np:NP107937.RAksOZxMlMmHkMVMnPV9RXXFmNw6SyaeNnVEGmVFRRSd4130_provenance
a
np:Provenance
.
dgn-np:NP107937.RAksOZxMlMmHkMVMnPV9RXXFmNw6SyaeNnVEGmVFRRSd4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP107937.RAksOZxMlMmHkMVMnPV9RXXFmNw6SyaeNnVEGmVFRRSd4130_assertion
{
miriam-gene:2153
a
ncit:C16612
.
lld:C0031542
a
ncit:C7057
.
dgn-gda:DGN2854ce0825d558b94415ee64a59e5428
sio:SIO_000628
miriam-gene:2153
,
lld:C0031542
;
a
sio:SIO_001122
.
}
dgn-np:NP107937.RAksOZxMlMmHkMVMnPV9RXXFmNw6SyaeNnVEGmVFRRSd4130_provenance
{
dgn-np:NP107937.RAksOZxMlMmHkMVMnPV9RXXFmNw6SyaeNnVEGmVFRRSd4130_assertion
dcterms:description
"[Our data demonstrate the high prevalence of these mutations, especially FV Leiden and associations, in patients with SVT on normal veins and their role in the progression to deep vein system.]. 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:18387654
;
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:NP107937.RAksOZxMlMmHkMVMnPV9RXXFmNw6SyaeNnVEGmVFRRSd4130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:39+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}