@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP939116.RAwHAP5Sx8e3uh1vEuVruDGVtqmfrAzC6y7hqRvEDwIv0
> .
@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:NP939116.RAwHAP5Sx8e3uh1vEuVruDGVtqmfrAzC6y7hqRvEDwIv0130_head
{
this:
np:hasAssertion
dgn-np:NP939116.RAwHAP5Sx8e3uh1vEuVruDGVtqmfrAzC6y7hqRvEDwIv0130_assertion
;
np:hasProvenance
dgn-np:NP939116.RAwHAP5Sx8e3uh1vEuVruDGVtqmfrAzC6y7hqRvEDwIv0130_provenance
;
np:hasPublicationInfo
dgn-np:NP939116.RAwHAP5Sx8e3uh1vEuVruDGVtqmfrAzC6y7hqRvEDwIv0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP939116.RAwHAP5Sx8e3uh1vEuVruDGVtqmfrAzC6y7hqRvEDwIv0130_assertion
a
np:Assertion
.
dgn-np:NP939116.RAwHAP5Sx8e3uh1vEuVruDGVtqmfrAzC6y7hqRvEDwIv0130_provenance
a
np:Provenance
.
dgn-np:NP939116.RAwHAP5Sx8e3uh1vEuVruDGVtqmfrAzC6y7hqRvEDwIv0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP939116.RAwHAP5Sx8e3uh1vEuVruDGVtqmfrAzC6y7hqRvEDwIv0130_assertion
{
miriam-gene:2153
a
ncit:C16612
.
lld:C0016522
a
ncit:C7057
.
dgn-gda:DGNd9ec00f8863aa9d6b168cb1678657f5f
sio:SIO_000628
miriam-gene:2153
,
lld:C0016522
;
a
sio:SIO_001121
.
}
dgn-np:NP939116.RAwHAP5Sx8e3uh1vEuVruDGVtqmfrAzC6y7hqRvEDwIv0130_provenance
{
dgn-np:NP939116.RAwHAP5Sx8e3uh1vEuVruDGVtqmfrAzC6y7hqRvEDwIv0130_assertion
dcterms:description
"[Further trends towards higher frequencies of the FVL mutation were found in patients with patent foramen ovale (OR 1.9), individual (OR 2.1) or family history of previous thrombembolisms (OR 2.0), and in those aged 25 years at onset of disease (OR 1.9, all not significant).]. 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:9776464
;
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:NP939116.RAwHAP5Sx8e3uh1vEuVruDGVtqmfrAzC6y7hqRvEDwIv0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:35+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" .
}