@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP624150.RA_bFwx7scU2lEqARNDis1ElqZMMWCD2DbUp1OdnXLqYQ
> .
@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:NP624150.RA_bFwx7scU2lEqARNDis1ElqZMMWCD2DbUp1OdnXLqYQ130_head
{
this:
np:hasAssertion
dgn-np:NP624150.RA_bFwx7scU2lEqARNDis1ElqZMMWCD2DbUp1OdnXLqYQ130_assertion
;
np:hasProvenance
dgn-np:NP624150.RA_bFwx7scU2lEqARNDis1ElqZMMWCD2DbUp1OdnXLqYQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP624150.RA_bFwx7scU2lEqARNDis1ElqZMMWCD2DbUp1OdnXLqYQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP624150.RA_bFwx7scU2lEqARNDis1ElqZMMWCD2DbUp1OdnXLqYQ130_assertion
a
np:Assertion
.
dgn-np:NP624150.RA_bFwx7scU2lEqARNDis1ElqZMMWCD2DbUp1OdnXLqYQ130_provenance
a
np:Provenance
.
dgn-np:NP624150.RA_bFwx7scU2lEqARNDis1ElqZMMWCD2DbUp1OdnXLqYQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP624150.RA_bFwx7scU2lEqARNDis1ElqZMMWCD2DbUp1OdnXLqYQ130_assertion
{
miriam-gene:8797
a
ncit:C16612
.
lld:C0030809
a
ncit:C7057
.
dgn-gda:DGN1c393a789515278140f71d628f3312c3
sio:SIO_000628
miriam-gene:8797
,
lld:C0030809
;
a
sio:SIO_001121
.
}
dgn-np:NP624150.RA_bFwx7scU2lEqARNDis1ElqZMMWCD2DbUp1OdnXLqYQ130_provenance
{
dgn-np:NP624150.RA_bFwx7scU2lEqARNDis1ElqZMMWCD2DbUp1OdnXLqYQ130_assertion
dcterms:description
"[Examination of the HLA antigens in this family indicates that there may be different variants of DR4, DQw3 and that one of them carried by the mother and son as part of the haplotype A30, B18, DR4, DQw3 is associated with pemphigus vulgaris.]. 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:2203658
;
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:NP624150.RA_bFwx7scU2lEqARNDis1ElqZMMWCD2DbUp1OdnXLqYQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:17+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" .
}