@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP571565.RAzBhWK980ib8vSJ-boWJj4DQm9ZiO4-ifzBV7r3IJuQs
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP571565.RAzBhWK980ib8vSJ-boWJj4DQm9ZiO4-ifzBV7r3IJuQs130_head
{
this:
np:hasAssertion
dgn-np:NP571565.RAzBhWK980ib8vSJ-boWJj4DQm9ZiO4-ifzBV7r3IJuQs130_assertion
;
np:hasProvenance
dgn-np:NP571565.RAzBhWK980ib8vSJ-boWJj4DQm9ZiO4-ifzBV7r3IJuQs130_provenance
;
np:hasPublicationInfo
dgn-np:NP571565.RAzBhWK980ib8vSJ-boWJj4DQm9ZiO4-ifzBV7r3IJuQs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP571565.RAzBhWK980ib8vSJ-boWJj4DQm9ZiO4-ifzBV7r3IJuQs130_assertion
a
np:Assertion
.
dgn-np:NP571565.RAzBhWK980ib8vSJ-boWJj4DQm9ZiO4-ifzBV7r3IJuQs130_provenance
a
np:Provenance
.
dgn-np:NP571565.RAzBhWK980ib8vSJ-boWJj4DQm9ZiO4-ifzBV7r3IJuQs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP571565.RAzBhWK980ib8vSJ-boWJj4DQm9ZiO4-ifzBV7r3IJuQs130_assertion
{
miriam-gene:4486
a
ncit:C16612
.
lld:C0014867
a
ncit:C7057
.
dgn-gda:DGN6e460d2048a9e60b1895412ea317cd8c
sio:SIO_000628
miriam-gene:4486
,
lld:C0014867
;
a
sio:SIO_001121
.
}
dgn-np:NP571565.RAzBhWK980ib8vSJ-boWJj4DQm9ZiO4-ifzBV7r3IJuQs130_provenance
{
dgn-np:NP571565.RAzBhWK980ib8vSJ-boWJj4DQm9ZiO4-ifzBV7r3IJuQs130_assertion
dcterms:description
"[This study suggested that high sCD163 levels and genetic risk variants are additional markers that can be combined with low platelet count to optimize assessment of EVs and bleeding in cirrhotic patients.]. 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:22849380
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP571565.RAzBhWK980ib8vSJ-boWJj4DQm9ZiO4-ifzBV7r3IJuQs130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:20+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}