@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP404121.RAEIg5v5UpMS1lUDtxTUX41UPPfh5FrFQdFbHu2QXzll8
> .
@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:NP404121.RAEIg5v5UpMS1lUDtxTUX41UPPfh5FrFQdFbHu2QXzll8130_head
{
this:
np:hasAssertion
dgn-np:NP404121.RAEIg5v5UpMS1lUDtxTUX41UPPfh5FrFQdFbHu2QXzll8130_assertion
;
np:hasProvenance
dgn-np:NP404121.RAEIg5v5UpMS1lUDtxTUX41UPPfh5FrFQdFbHu2QXzll8130_provenance
;
np:hasPublicationInfo
dgn-np:NP404121.RAEIg5v5UpMS1lUDtxTUX41UPPfh5FrFQdFbHu2QXzll8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP404121.RAEIg5v5UpMS1lUDtxTUX41UPPfh5FrFQdFbHu2QXzll8130_assertion
a
np:Assertion
.
dgn-np:NP404121.RAEIg5v5UpMS1lUDtxTUX41UPPfh5FrFQdFbHu2QXzll8130_provenance
a
np:Provenance
.
dgn-np:NP404121.RAEIg5v5UpMS1lUDtxTUX41UPPfh5FrFQdFbHu2QXzll8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP404121.RAEIg5v5UpMS1lUDtxTUX41UPPfh5FrFQdFbHu2QXzll8130_assertion
{
miriam-gene:1351
a
ncit:C16612
.
lld:C0040038
a
ncit:C7057
.
dgn-gda:DGN0a9f91514ff2d381d6904518780da829
sio:SIO_000628
miriam-gene:1351
,
lld:C0040038
;
a
sio:SIO_001121
.
}
dgn-np:NP404121.RAEIg5v5UpMS1lUDtxTUX41UPPfh5FrFQdFbHu2QXzll8130_provenance
{
dgn-np:NP404121.RAEIg5v5UpMS1lUDtxTUX41UPPfh5FrFQdFbHu2QXzll8130_assertion
dcterms:description
"[Here we have analysed 125 consecutive patients with incidental or recurrent venous thromboembolism for the presence of mutations at the cleavage sites for APC at amino acid positions Arg336 and Arg562 of factor VIII.]. 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:8616046
;
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:NP404121.RAEIg5v5UpMS1lUDtxTUX41UPPfh5FrFQdFbHu2QXzll8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:00+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" .
}