@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP666043.RAzNJF6TA9n48LSZCmgJ9e1W8VrYmeb5mh1ZbMmw7OsCE
> .
@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:NP666043.RAzNJF6TA9n48LSZCmgJ9e1W8VrYmeb5mh1ZbMmw7OsCE130_head
{
this:
np:hasAssertion
dgn-np:NP666043.RAzNJF6TA9n48LSZCmgJ9e1W8VrYmeb5mh1ZbMmw7OsCE130_assertion
;
np:hasProvenance
dgn-np:NP666043.RAzNJF6TA9n48LSZCmgJ9e1W8VrYmeb5mh1ZbMmw7OsCE130_provenance
;
np:hasPublicationInfo
dgn-np:NP666043.RAzNJF6TA9n48LSZCmgJ9e1W8VrYmeb5mh1ZbMmw7OsCE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP666043.RAzNJF6TA9n48LSZCmgJ9e1W8VrYmeb5mh1ZbMmw7OsCE130_assertion
a
np:Assertion
.
dgn-np:NP666043.RAzNJF6TA9n48LSZCmgJ9e1W8VrYmeb5mh1ZbMmw7OsCE130_provenance
a
np:Provenance
.
dgn-np:NP666043.RAzNJF6TA9n48LSZCmgJ9e1W8VrYmeb5mh1ZbMmw7OsCE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP666043.RAzNJF6TA9n48LSZCmgJ9e1W8VrYmeb5mh1ZbMmw7OsCE130_assertion
{
miriam-gene:100293534
a
ncit:C16612
.
lld:C0001627
a
ncit:C7057
.
dgn-gda:DGNa92988722238928c6ca11fc4ce3d08d6
sio:SIO_000628
miriam-gene:100293534
,
lld:C0001627
;
a
sio:SIO_001121
.
}
dgn-np:NP666043.RAzNJF6TA9n48LSZCmgJ9e1W8VrYmeb5mh1ZbMmw7OsCE130_provenance
{
dgn-np:NP666043.RAzNJF6TA9n48LSZCmgJ9e1W8VrYmeb5mh1ZbMmw7OsCE130_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:NP666043.RAzNJF6TA9n48LSZCmgJ9e1W8VrYmeb5mh1ZbMmw7OsCE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:42+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" .
}