@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP507155.RAgmuMmOx55FytiX3AMypB8gfovIUgc9CanbVIxRQs7c8
> .
@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:NP507155.RAgmuMmOx55FytiX3AMypB8gfovIUgc9CanbVIxRQs7c8130_head
{
this:
np:hasAssertion
dgn-np:NP507155.RAgmuMmOx55FytiX3AMypB8gfovIUgc9CanbVIxRQs7c8130_assertion
;
np:hasProvenance
dgn-np:NP507155.RAgmuMmOx55FytiX3AMypB8gfovIUgc9CanbVIxRQs7c8130_provenance
;
np:hasPublicationInfo
dgn-np:NP507155.RAgmuMmOx55FytiX3AMypB8gfovIUgc9CanbVIxRQs7c8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP507155.RAgmuMmOx55FytiX3AMypB8gfovIUgc9CanbVIxRQs7c8130_assertion
a
np:Assertion
.
dgn-np:NP507155.RAgmuMmOx55FytiX3AMypB8gfovIUgc9CanbVIxRQs7c8130_provenance
a
np:Provenance
.
dgn-np:NP507155.RAgmuMmOx55FytiX3AMypB8gfovIUgc9CanbVIxRQs7c8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP507155.RAgmuMmOx55FytiX3AMypB8gfovIUgc9CanbVIxRQs7c8130_assertion
{
miriam-gene:2147
a
ncit:C16612
.
lld:C0023890
a
ncit:C7057
.
dgn-gda:DGN89de839f203eb5117a124f6708741482
sio:SIO_000628
miriam-gene:2147
,
lld:C0023890
;
a
sio:SIO_001121
.
}
dgn-np:NP507155.RAgmuMmOx55FytiX3AMypB8gfovIUgc9CanbVIxRQs7c8130_provenance
{
dgn-np:NP507155.RAgmuMmOx55FytiX3AMypB8gfovIUgc9CanbVIxRQs7c8130_assertion
dcterms:description
"[We studied thrombophilic genetic factors (TGFs) MTHFR C677TT, PAI1 4G-4G, V Leiden Q506, prothrombin G20210A as risk factors in 94 patients with HCC with and without portal vein thrombosis (PVT), compared with 214 patients with liver cirrhosis (LC) with and without PVT and 94 healthy controls (HC).]. 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:18618228
;
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:NP507155.RAgmuMmOx55FytiX3AMypB8gfovIUgc9CanbVIxRQs7c8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:02+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" .
}