@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP242731.RAScza1WkCWPrdv1-0Iw_t43cVdwgzbJLSUp0vUwoRAW4
> .
@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:NP242731.RAScza1WkCWPrdv1-0Iw_t43cVdwgzbJLSUp0vUwoRAW4130_head
{
this:
np:hasAssertion
dgn-np:NP242731.RAScza1WkCWPrdv1-0Iw_t43cVdwgzbJLSUp0vUwoRAW4130_assertion
;
np:hasProvenance
dgn-np:NP242731.RAScza1WkCWPrdv1-0Iw_t43cVdwgzbJLSUp0vUwoRAW4130_provenance
;
np:hasPublicationInfo
dgn-np:NP242731.RAScza1WkCWPrdv1-0Iw_t43cVdwgzbJLSUp0vUwoRAW4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP242731.RAScza1WkCWPrdv1-0Iw_t43cVdwgzbJLSUp0vUwoRAW4130_assertion
a
np:Assertion
.
dgn-np:NP242731.RAScza1WkCWPrdv1-0Iw_t43cVdwgzbJLSUp0vUwoRAW4130_provenance
a
np:Provenance
.
dgn-np:NP242731.RAScza1WkCWPrdv1-0Iw_t43cVdwgzbJLSUp0vUwoRAW4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP242731.RAScza1WkCWPrdv1-0Iw_t43cVdwgzbJLSUp0vUwoRAW4130_assertion
{
miriam-gene:2153
a
ncit:C16612
.
lld:C1458156
a
ncit:C7057
.
dgn-gda:DGN756639cf7c0f6c4243c8070bc731ce3b
sio:SIO_000628
miriam-gene:2153
,
lld:C1458156
;
a
sio:SIO_001121
.
}
dgn-np:NP242731.RAScza1WkCWPrdv1-0Iw_t43cVdwgzbJLSUp0vUwoRAW4130_provenance
{
dgn-np:NP242731.RAScza1WkCWPrdv1-0Iw_t43cVdwgzbJLSUp0vUwoRAW4130_assertion
dcterms:description
"[The evidence is insufficient to draw conclusions about excess VTE recurrence risk resulting from compound heterozygosity (FVL and PT), but it is likely to be at least as high as with FVL alone.]. 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:21150787
;
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:NP242731.RAScza1WkCWPrdv1-0Iw_t43cVdwgzbJLSUp0vUwoRAW4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:16+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" .
}