@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP137903.RApllT19F43IzPHR6pGpLROmvIEbnuhV86T6rEAFwouaA
> .
@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:NP137903.RApllT19F43IzPHR6pGpLROmvIEbnuhV86T6rEAFwouaA130_head
{
this:
np:hasAssertion
dgn-np:NP137903.RApllT19F43IzPHR6pGpLROmvIEbnuhV86T6rEAFwouaA130_assertion
;
np:hasProvenance
dgn-np:NP137903.RApllT19F43IzPHR6pGpLROmvIEbnuhV86T6rEAFwouaA130_provenance
;
np:hasPublicationInfo
dgn-np:NP137903.RApllT19F43IzPHR6pGpLROmvIEbnuhV86T6rEAFwouaA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP137903.RApllT19F43IzPHR6pGpLROmvIEbnuhV86T6rEAFwouaA130_assertion
a
np:Assertion
.
dgn-np:NP137903.RApllT19F43IzPHR6pGpLROmvIEbnuhV86T6rEAFwouaA130_provenance
a
np:Provenance
.
dgn-np:NP137903.RApllT19F43IzPHR6pGpLROmvIEbnuhV86T6rEAFwouaA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP137903.RApllT19F43IzPHR6pGpLROmvIEbnuhV86T6rEAFwouaA130_assertion
{
miriam-gene:2200
a
ncit:C16612
.
lld:C0036421
a
ncit:C7057
.
dgn-gda:DGN0fe1641b122c538dd8778d29290404af
sio:SIO_000628
miriam-gene:2200
,
lld:C0036421
;
a
sio:SIO_001123
.
}
dgn-np:NP137903.RApllT19F43IzPHR6pGpLROmvIEbnuhV86T6rEAFwouaA130_provenance
{
dgn-np:NP137903.RApllT19F43IzPHR6pGpLROmvIEbnuhV86T6rEAFwouaA130_assertion
dcterms:description
"[AECA subsets in the sera of patients with systemic sclerosis (SSc) and diffuse SSc induce patterns of human dermal endothelial cells gene expression in the setting of apoptosis with increased caspase 3 activity and reexpression of fibrillin 1.]. 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:16802364
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP137903.RApllT19F43IzPHR6pGpLROmvIEbnuhV86T6rEAFwouaA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:12+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" .
}