@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP198719.RAJxc9V1rQfJnWZgmEe7HWWlfHfzks014WdOi13mmNdzE
> .
@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:NP198719.RAJxc9V1rQfJnWZgmEe7HWWlfHfzks014WdOi13mmNdzE130_head
{
this:
np:hasAssertion
dgn-np:NP198719.RAJxc9V1rQfJnWZgmEe7HWWlfHfzks014WdOi13mmNdzE130_assertion
;
np:hasProvenance
dgn-np:NP198719.RAJxc9V1rQfJnWZgmEe7HWWlfHfzks014WdOi13mmNdzE130_provenance
;
np:hasPublicationInfo
dgn-np:NP198719.RAJxc9V1rQfJnWZgmEe7HWWlfHfzks014WdOi13mmNdzE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP198719.RAJxc9V1rQfJnWZgmEe7HWWlfHfzks014WdOi13mmNdzE130_assertion
a
np:Assertion
.
dgn-np:NP198719.RAJxc9V1rQfJnWZgmEe7HWWlfHfzks014WdOi13mmNdzE130_provenance
a
np:Provenance
.
dgn-np:NP198719.RAJxc9V1rQfJnWZgmEe7HWWlfHfzks014WdOi13mmNdzE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP198719.RAJxc9V1rQfJnWZgmEe7HWWlfHfzks014WdOi13mmNdzE130_assertion
{
miriam-gene:721
a
ncit:C16612
.
lld:C0024141
a
ncit:C7057
.
dgn-gda:DGNce6b0bff56bd78a923f8c6a7b2f201a9
sio:SIO_000628
miriam-gene:721
,
lld:C0024141
;
a
sio:SIO_001121
.
}
dgn-np:NP198719.RAJxc9V1rQfJnWZgmEe7HWWlfHfzks014WdOi13mmNdzE130_provenance
{
dgn-np:NP198719.RAJxc9V1rQfJnWZgmEe7HWWlfHfzks014WdOi13mmNdzE130_assertion
dcterms:description
"[HLA-B8, DR3 and C4A null phenotypes occurred frequently in Caucasian patients with CTD, especially those with systemic lupus erythematosus (SLE), but were also more commonly found among healthy white controls of this southeast Georgia community.]. 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:1976808
;
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:NP198719.RAJxc9V1rQfJnWZgmEe7HWWlfHfzks014WdOi13mmNdzE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:49+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" .
}