@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP47706.RA3ypHGOkX4Q1oDrH9OU-tKJF7NHuddKBslmobSHiFvQQ
> .
@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:NP47706.RA3ypHGOkX4Q1oDrH9OU-tKJF7NHuddKBslmobSHiFvQQ130_head
{
this:
np:hasAssertion
dgn-np:NP47706.RA3ypHGOkX4Q1oDrH9OU-tKJF7NHuddKBslmobSHiFvQQ130_assertion
;
np:hasProvenance
dgn-np:NP47706.RA3ypHGOkX4Q1oDrH9OU-tKJF7NHuddKBslmobSHiFvQQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP47706.RA3ypHGOkX4Q1oDrH9OU-tKJF7NHuddKBslmobSHiFvQQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP47706.RA3ypHGOkX4Q1oDrH9OU-tKJF7NHuddKBslmobSHiFvQQ130_assertion
a
np:Assertion
.
dgn-np:NP47706.RA3ypHGOkX4Q1oDrH9OU-tKJF7NHuddKBslmobSHiFvQQ130_provenance
a
np:Provenance
.
dgn-np:NP47706.RA3ypHGOkX4Q1oDrH9OU-tKJF7NHuddKBslmobSHiFvQQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP47706.RA3ypHGOkX4Q1oDrH9OU-tKJF7NHuddKBslmobSHiFvQQ130_assertion
{
miriam-gene:717
a
ncit:C16612
.
lld:C1258104
a
ncit:C7057
.
dgn-gda:DGNadf9052b6afd439b0e40135bc377dba6
sio:SIO_000628
miriam-gene:717
,
lld:C1258104
;
a
sio:SIO_001122
.
}
dgn-np:NP47706.RA3ypHGOkX4Q1oDrH9OU-tKJF7NHuddKBslmobSHiFvQQ130_provenance
{
dgn-np:NP47706.RA3ypHGOkX4Q1oDrH9OU-tKJF7NHuddKBslmobSHiFvQQ130_assertion
dcterms:description
"[Deficiency of the complement component C4 at the functional, protein and gene level and deficiency of complement component C2 at the functional level were investigated and HLA analysis was performed on patients with limited and diffuse systemic sclerosis (SSc).]. 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:9691203
;
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:NP47706.RA3ypHGOkX4Q1oDrH9OU-tKJF7NHuddKBslmobSHiFvQQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}