@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP51147.RAisIvEPd6LicP8qpGKRpcYM2roBDe7qc0_NXYePOb6iY
> .
@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:NP51147.RAisIvEPd6LicP8qpGKRpcYM2roBDe7qc0_NXYePOb6iY130_head
{
this:
np:hasAssertion
dgn-np:NP51147.RAisIvEPd6LicP8qpGKRpcYM2roBDe7qc0_NXYePOb6iY130_assertion
;
np:hasProvenance
dgn-np:NP51147.RAisIvEPd6LicP8qpGKRpcYM2roBDe7qc0_NXYePOb6iY130_provenance
;
np:hasPublicationInfo
dgn-np:NP51147.RAisIvEPd6LicP8qpGKRpcYM2roBDe7qc0_NXYePOb6iY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP51147.RAisIvEPd6LicP8qpGKRpcYM2roBDe7qc0_NXYePOb6iY130_assertion
a
np:Assertion
.
dgn-np:NP51147.RAisIvEPd6LicP8qpGKRpcYM2roBDe7qc0_NXYePOb6iY130_provenance
a
np:Provenance
.
dgn-np:NP51147.RAisIvEPd6LicP8qpGKRpcYM2roBDe7qc0_NXYePOb6iY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP51147.RAisIvEPd6LicP8qpGKRpcYM2roBDe7qc0_NXYePOb6iY130_assertion
{
miriam-gene:6678
a
ncit:C16612
.
lld:C0011644
a
ncit:C7057
.
dgn-gda:DGNe6f3e8abbd001c94e88a1a8f3847650e
sio:SIO_000628
miriam-gene:6678
,
lld:C0011644
;
a
sio:SIO_001122
.
}
dgn-np:NP51147.RAisIvEPd6LicP8qpGKRpcYM2roBDe7qc0_NXYePOb6iY130_provenance
{
dgn-np:NP51147.RAisIvEPd6LicP8qpGKRpcYM2roBDe7qc0_NXYePOb6iY130_assertion
dcterms:description
"[ This study is the first to show that polymorphisms of the SPARC gene are associated with susceptibility to, and clinical manifestations of, SSc and that they may also be functionally important in influencing SPARC expression in skin fibroblasts.]. 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:12428242
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP51147.RAisIvEPd6LicP8qpGKRpcYM2roBDe7qc0_NXYePOb6iY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:23+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" .
}