@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP184629.RAUCZUCDYqOpUpCmDwUeY2cCH4WmC37mQmJM592AdvIy8
> .
@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:NP184629.RAUCZUCDYqOpUpCmDwUeY2cCH4WmC37mQmJM592AdvIy8130_head
{
this:
np:hasAssertion
dgn-np:NP184629.RAUCZUCDYqOpUpCmDwUeY2cCH4WmC37mQmJM592AdvIy8130_assertion
;
np:hasProvenance
dgn-np:NP184629.RAUCZUCDYqOpUpCmDwUeY2cCH4WmC37mQmJM592AdvIy8130_provenance
;
np:hasPublicationInfo
dgn-np:NP184629.RAUCZUCDYqOpUpCmDwUeY2cCH4WmC37mQmJM592AdvIy8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP184629.RAUCZUCDYqOpUpCmDwUeY2cCH4WmC37mQmJM592AdvIy8130_assertion
a
np:Assertion
.
dgn-np:NP184629.RAUCZUCDYqOpUpCmDwUeY2cCH4WmC37mQmJM592AdvIy8130_provenance
a
np:Provenance
.
dgn-np:NP184629.RAUCZUCDYqOpUpCmDwUeY2cCH4WmC37mQmJM592AdvIy8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP184629.RAUCZUCDYqOpUpCmDwUeY2cCH4WmC37mQmJM592AdvIy8130_assertion
{
miriam-gene:1589
a
ncit:C16612
.
lld:C0004364
a
ncit:C7057
.
dgn-gda:DGNeb8f98c4c055c0b8ebe3da62f47c9e4f
sio:SIO_000628
miriam-gene:1589
,
lld:C0004364
;
a
sio:SIO_001121
.
}
dgn-np:NP184629.RAUCZUCDYqOpUpCmDwUeY2cCH4WmC37mQmJM592AdvIy8130_provenance
{
dgn-np:NP184629.RAUCZUCDYqOpUpCmDwUeY2cCH4WmC37mQmJM592AdvIy8130_assertion
dcterms:description
"[Several autoimmune disorders as well as congenital adrenal hyperplasia (CAH) are either associated or closely linked with genetic variants of the fourth component of complement (C4A and C4B) and the enzyme steroid 21-hydroxylase (21-OH).]. 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:3018042
;
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:NP184629.RAUCZUCDYqOpUpCmDwUeY2cCH4WmC37mQmJM592AdvIy8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:40+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" .
}