@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP134440.RAziF102FeXYeiPWbpwcg0xYrNTS_KkcCqywn6M165Myw
> .
@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:NP134440.RAziF102FeXYeiPWbpwcg0xYrNTS_KkcCqywn6M165Myw130_head
{
this:
np:hasAssertion
dgn-np:NP134440.RAziF102FeXYeiPWbpwcg0xYrNTS_KkcCqywn6M165Myw130_assertion
;
np:hasProvenance
dgn-np:NP134440.RAziF102FeXYeiPWbpwcg0xYrNTS_KkcCqywn6M165Myw130_provenance
;
np:hasPublicationInfo
dgn-np:NP134440.RAziF102FeXYeiPWbpwcg0xYrNTS_KkcCqywn6M165Myw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP134440.RAziF102FeXYeiPWbpwcg0xYrNTS_KkcCqywn6M165Myw130_assertion
a
np:Assertion
.
dgn-np:NP134440.RAziF102FeXYeiPWbpwcg0xYrNTS_KkcCqywn6M165Myw130_provenance
a
np:Provenance
.
dgn-np:NP134440.RAziF102FeXYeiPWbpwcg0xYrNTS_KkcCqywn6M165Myw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP134440.RAziF102FeXYeiPWbpwcg0xYrNTS_KkcCqywn6M165Myw130_assertion
{
miriam-gene:2153
a
ncit:C16612
.
lld:C0040053
a
ncit:C7057
.
dgn-gda:DGN07d506ea4e469abd357bf3677c7f643c
sio:SIO_000628
miriam-gene:2153
,
lld:C0040053
;
a
sio:SIO_001123
.
}
dgn-np:NP134440.RAziF102FeXYeiPWbpwcg0xYrNTS_KkcCqywn6M165Myw130_provenance
{
dgn-np:NP134440.RAziF102FeXYeiPWbpwcg0xYrNTS_KkcCqywn6M165Myw130_assertion
dcterms:description
"[FV Leiden prevalence is quite high and coexistence of FV Leiden with other hereditary causes of thrombosis such as prothrombin G20210A mutation methylenetetrahydrofolate reductase 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:NP134440.RAziF102FeXYeiPWbpwcg0xYrNTS_KkcCqywn6M165Myw130_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" .
}