@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP298754.RAJqG5fENTXB5q_5KT7JHVJCzD6xIXo9DdDFdjQLymt0s
> .
@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:NP298754.RAJqG5fENTXB5q_5KT7JHVJCzD6xIXo9DdDFdjQLymt0s130_head
{
this:
np:hasAssertion
dgn-np:NP298754.RAJqG5fENTXB5q_5KT7JHVJCzD6xIXo9DdDFdjQLymt0s130_assertion
;
np:hasProvenance
dgn-np:NP298754.RAJqG5fENTXB5q_5KT7JHVJCzD6xIXo9DdDFdjQLymt0s130_provenance
;
np:hasPublicationInfo
dgn-np:NP298754.RAJqG5fENTXB5q_5KT7JHVJCzD6xIXo9DdDFdjQLymt0s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP298754.RAJqG5fENTXB5q_5KT7JHVJCzD6xIXo9DdDFdjQLymt0s130_assertion
a
np:Assertion
.
dgn-np:NP298754.RAJqG5fENTXB5q_5KT7JHVJCzD6xIXo9DdDFdjQLymt0s130_provenance
a
np:Provenance
.
dgn-np:NP298754.RAJqG5fENTXB5q_5KT7JHVJCzD6xIXo9DdDFdjQLymt0s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP298754.RAJqG5fENTXB5q_5KT7JHVJCzD6xIXo9DdDFdjQLymt0s130_assertion
{
miriam-gene:1361
a
ncit:C16612
.
lld:C0600433
a
ncit:C7057
.
dgn-gda:DGN8007002c70d38108773c55578d535574
sio:SIO_000628
miriam-gene:1361
,
lld:C0600433
;
a
sio:SIO_001121
.
}
dgn-np:NP298754.RAJqG5fENTXB5q_5KT7JHVJCzD6xIXo9DdDFdjQLymt0s130_provenance
{
dgn-np:NP298754.RAJqG5fENTXB5q_5KT7JHVJCzD6xIXo9DdDFdjQLymt0s130_assertion
dcterms:description
"[It is suggested that APC resistance caused by hyperprothrombinaemia does not translate in impaired fibrinolysis, at least in the presence of high APC levels, because the increase in thrombin formation is insufficient to activate the amount of TAFI required to inhibit plasminogen conversion.]. 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:16601829
;
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:NP298754.RAJqG5fENTXB5q_5KT7JHVJCzD6xIXo9DdDFdjQLymt0s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:49+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" .
}