@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP453622.RAXhXXePbytLTsCwFNKjzyigkrrqmue310qGLx6zq5O24
> .
@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:NP453622.RAXhXXePbytLTsCwFNKjzyigkrrqmue310qGLx6zq5O24130_head
{
this:
np:hasAssertion
dgn-np:NP453622.RAXhXXePbytLTsCwFNKjzyigkrrqmue310qGLx6zq5O24130_assertion
;
np:hasProvenance
dgn-np:NP453622.RAXhXXePbytLTsCwFNKjzyigkrrqmue310qGLx6zq5O24130_provenance
;
np:hasPublicationInfo
dgn-np:NP453622.RAXhXXePbytLTsCwFNKjzyigkrrqmue310qGLx6zq5O24130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP453622.RAXhXXePbytLTsCwFNKjzyigkrrqmue310qGLx6zq5O24130_assertion
a
np:Assertion
.
dgn-np:NP453622.RAXhXXePbytLTsCwFNKjzyigkrrqmue310qGLx6zq5O24130_provenance
a
np:Provenance
.
dgn-np:NP453622.RAXhXXePbytLTsCwFNKjzyigkrrqmue310qGLx6zq5O24130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP453622.RAXhXXePbytLTsCwFNKjzyigkrrqmue310qGLx6zq5O24130_assertion
{
miriam-gene:3053
a
ncit:C16612
.
lld:C0398623
a
ncit:C7057
.
dgn-gda:DGN1d0df96740f1cd1b214ff3e03a786ebd
sio:SIO_000628
miriam-gene:3053
,
lld:C0398623
;
a
sio:SIO_001121
.
}
dgn-np:NP453622.RAXhXXePbytLTsCwFNKjzyigkrrqmue310qGLx6zq5O24130_provenance
{
dgn-np:NP453622.RAXhXXePbytLTsCwFNKjzyigkrrqmue310qGLx6zq5O24130_assertion
dcterms:description
"[The tests included in the second step of the screening are aimed at detecting the less common or less well established causes of inherited thrombophilia (low heparin cofactor II, defective release of tissue plasminogen activator, and high plasminogen activator inhibitor).]. 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:3116699
;
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:NP453622.RAXhXXePbytLTsCwFNKjzyigkrrqmue310qGLx6zq5O24130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:30+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" .
}