@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP640216.RAnRXRsA-UgUfrVsy2jIPxv1mipDJIVVPWtSCbg5UO7AE
> .
@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:NP640216.RAnRXRsA-UgUfrVsy2jIPxv1mipDJIVVPWtSCbg5UO7AE130_head
{
this:
np:hasAssertion
dgn-np:NP640216.RAnRXRsA-UgUfrVsy2jIPxv1mipDJIVVPWtSCbg5UO7AE130_assertion
;
np:hasProvenance
dgn-np:NP640216.RAnRXRsA-UgUfrVsy2jIPxv1mipDJIVVPWtSCbg5UO7AE130_provenance
;
np:hasPublicationInfo
dgn-np:NP640216.RAnRXRsA-UgUfrVsy2jIPxv1mipDJIVVPWtSCbg5UO7AE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP640216.RAnRXRsA-UgUfrVsy2jIPxv1mipDJIVVPWtSCbg5UO7AE130_assertion
a
np:Assertion
.
dgn-np:NP640216.RAnRXRsA-UgUfrVsy2jIPxv1mipDJIVVPWtSCbg5UO7AE130_provenance
a
np:Provenance
.
dgn-np:NP640216.RAnRXRsA-UgUfrVsy2jIPxv1mipDJIVVPWtSCbg5UO7AE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP640216.RAnRXRsA-UgUfrVsy2jIPxv1mipDJIVVPWtSCbg5UO7AE130_assertion
{
miriam-gene:940
a
ncit:C16612
.
lld:C0036421
a
ncit:C7057
.
dgn-gda:DGN52c772f279d4108fb1e878761541c096
sio:SIO_000628
miriam-gene:940
,
lld:C0036421
;
a
sio:SIO_001121
.
}
dgn-np:NP640216.RAnRXRsA-UgUfrVsy2jIPxv1mipDJIVVPWtSCbg5UO7AE130_provenance
{
dgn-np:NP640216.RAnRXRsA-UgUfrVsy2jIPxv1mipDJIVVPWtSCbg5UO7AE130_assertion
dcterms:description
"[Cellular microchimerism was found in SSc patients and controls, but the absolute amount of male DNA was higher in the patients, and the in vitro addition to blood mononuclear cells of an anti-CD28 costimulatory signal acted as a powerful amplification of microchimeric cells in 3 patients with SSc but not in controls.]. 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:12687555
;
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:NP640216.RAnRXRsA-UgUfrVsy2jIPxv1mipDJIVVPWtSCbg5UO7AE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:26+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" .
}