@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP134443.RATKoWs7mk6EyJQhVYR2aQk4J95eH2By0tDwCA6KZLqrg
> .
@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:NP134443.RATKoWs7mk6EyJQhVYR2aQk4J95eH2By0tDwCA6KZLqrg130_head
{
this:
np:hasAssertion
dgn-np:NP134443.RATKoWs7mk6EyJQhVYR2aQk4J95eH2By0tDwCA6KZLqrg130_assertion
;
np:hasProvenance
dgn-np:NP134443.RATKoWs7mk6EyJQhVYR2aQk4J95eH2By0tDwCA6KZLqrg130_provenance
;
np:hasPublicationInfo
dgn-np:NP134443.RATKoWs7mk6EyJQhVYR2aQk4J95eH2By0tDwCA6KZLqrg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP134443.RATKoWs7mk6EyJQhVYR2aQk4J95eH2By0tDwCA6KZLqrg130_assertion
a
np:Assertion
.
dgn-np:NP134443.RATKoWs7mk6EyJQhVYR2aQk4J95eH2By0tDwCA6KZLqrg130_provenance
a
np:Provenance
.
dgn-np:NP134443.RATKoWs7mk6EyJQhVYR2aQk4J95eH2By0tDwCA6KZLqrg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP134443.RATKoWs7mk6EyJQhVYR2aQk4J95eH2By0tDwCA6KZLqrg130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0040053
a
ncit:C7057
.
dgn-gda:DGNcc7dd46cab4a5b79be9be8ca7eb8900d
sio:SIO_000628
miriam-gene:4524
,
lld:C0040053
;
a
sio:SIO_001123
.
}
dgn-np:NP134443.RATKoWs7mk6EyJQhVYR2aQk4J95eH2By0tDwCA6KZLqrg130_provenance
{
dgn-np:NP134443.RATKoWs7mk6EyJQhVYR2aQk4J95eH2By0tDwCA6KZLqrg130_assertion
dcterms:description
"[factor V (FV) Leiden prevalence is quite high and coexistence of FV Leiden with other hereditary causes of thrombosis such as prothrombin G20210A mutation MTHFR enzyme defect is not rare in healthy population of Aegean region of Turkey ]. 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:17456626
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP134443.RATKoWs7mk6EyJQhVYR2aQk4J95eH2By0tDwCA6KZLqrg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:10+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" .
}