@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP907582.RAclJLUkS3BbE5X-TPlW8D-oKnYqzGmgIcI37MBgDPV-o
> .
@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:NP907582.RAclJLUkS3BbE5X-TPlW8D-oKnYqzGmgIcI37MBgDPV-o130_head
{
this:
np:hasAssertion
dgn-np:NP907582.RAclJLUkS3BbE5X-TPlW8D-oKnYqzGmgIcI37MBgDPV-o130_assertion
;
np:hasProvenance
dgn-np:NP907582.RAclJLUkS3BbE5X-TPlW8D-oKnYqzGmgIcI37MBgDPV-o130_provenance
;
np:hasPublicationInfo
dgn-np:NP907582.RAclJLUkS3BbE5X-TPlW8D-oKnYqzGmgIcI37MBgDPV-o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP907582.RAclJLUkS3BbE5X-TPlW8D-oKnYqzGmgIcI37MBgDPV-o130_assertion
a
np:Assertion
.
dgn-np:NP907582.RAclJLUkS3BbE5X-TPlW8D-oKnYqzGmgIcI37MBgDPV-o130_provenance
a
np:Provenance
.
dgn-np:NP907582.RAclJLUkS3BbE5X-TPlW8D-oKnYqzGmgIcI37MBgDPV-o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP907582.RAclJLUkS3BbE5X-TPlW8D-oKnYqzGmgIcI37MBgDPV-o130_assertion
{
miriam-gene:3053
a
ncit:C16612
.
lld:C0149871
a
ncit:C7057
.
dgn-gda:DGNd7cf18b67aa95f36627dcad287d55f98
sio:SIO_000628
miriam-gene:3053
,
lld:C0149871
;
a
sio:SIO_001121
.
}
dgn-np:NP907582.RAclJLUkS3BbE5X-TPlW8D-oKnYqzGmgIcI37MBgDPV-o130_provenance
{
dgn-np:NP907582.RAclJLUkS3BbE5X-TPlW8D-oKnYqzGmgIcI37MBgDPV-o130_assertion
dcterms:description
"[Although there have been reports on families in which a heterozygous HCII deficiency is associated with thromboembolic events, several epidemiological studies revealed that heterozygous HCII deficiency is as prevalent among healthy subjects as it is among patients with deep venous thrombosis (DVT).]. 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:10494755
;
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:NP907582.RAclJLUkS3BbE5X-TPlW8D-oKnYqzGmgIcI37MBgDPV-o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:17+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" .
}