@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP608349.RAqFZxV7hPfuSMAhj13q-5x-aKezglIdU93N29swzbpCs
> .
@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:NP608349.RAqFZxV7hPfuSMAhj13q-5x-aKezglIdU93N29swzbpCs130_head
{
this:
np:hasAssertion
dgn-np:NP608349.RAqFZxV7hPfuSMAhj13q-5x-aKezglIdU93N29swzbpCs130_assertion
;
np:hasProvenance
dgn-np:NP608349.RAqFZxV7hPfuSMAhj13q-5x-aKezglIdU93N29swzbpCs130_provenance
;
np:hasPublicationInfo
dgn-np:NP608349.RAqFZxV7hPfuSMAhj13q-5x-aKezglIdU93N29swzbpCs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP608349.RAqFZxV7hPfuSMAhj13q-5x-aKezglIdU93N29swzbpCs130_assertion
a
np:Assertion
.
dgn-np:NP608349.RAqFZxV7hPfuSMAhj13q-5x-aKezglIdU93N29swzbpCs130_provenance
a
np:Provenance
.
dgn-np:NP608349.RAqFZxV7hPfuSMAhj13q-5x-aKezglIdU93N29swzbpCs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP608349.RAqFZxV7hPfuSMAhj13q-5x-aKezglIdU93N29swzbpCs130_assertion
{
miriam-gene:5660
a
ncit:C16612
.
lld:C1859616
a
ncit:C7057
.
dgn-gda:DGNc57705b9fdf5713aecb08944b2803a6b
sio:SIO_000628
miriam-gene:5660
,
lld:C1859616
;
a
sio:SIO_001121
.
}
dgn-np:NP608349.RAqFZxV7hPfuSMAhj13q-5x-aKezglIdU93N29swzbpCs130_provenance
{
dgn-np:NP608349.RAqFZxV7hPfuSMAhj13q-5x-aKezglIdU93N29swzbpCs130_assertion
dcterms:description
"[Whether hereditary protein S, protein C, or antithrombin deficiency is associated with arterial thromboembolism (ATE) and whether history of venous thromboembolism in these subjects predisposes them to subsequent ATE have yet to be determined.]. 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:18824642
;
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:NP608349.RAqFZxV7hPfuSMAhj13q-5x-aKezglIdU93N29swzbpCs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:05+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" .
}