@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP501885.RAGK9gzpGGVPWZWnuBUFhHQ_TY3VYJ0NZXTh6woO9pM_M
> .
@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:NP501885.RAGK9gzpGGVPWZWnuBUFhHQ_TY3VYJ0NZXTh6woO9pM_M130_head
{
this:
np:hasAssertion
dgn-np:NP501885.RAGK9gzpGGVPWZWnuBUFhHQ_TY3VYJ0NZXTh6woO9pM_M130_assertion
;
np:hasProvenance
dgn-np:NP501885.RAGK9gzpGGVPWZWnuBUFhHQ_TY3VYJ0NZXTh6woO9pM_M130_provenance
;
np:hasPublicationInfo
dgn-np:NP501885.RAGK9gzpGGVPWZWnuBUFhHQ_TY3VYJ0NZXTh6woO9pM_M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP501885.RAGK9gzpGGVPWZWnuBUFhHQ_TY3VYJ0NZXTh6woO9pM_M130_assertion
a
np:Assertion
.
dgn-np:NP501885.RAGK9gzpGGVPWZWnuBUFhHQ_TY3VYJ0NZXTh6woO9pM_M130_provenance
a
np:Provenance
.
dgn-np:NP501885.RAGK9gzpGGVPWZWnuBUFhHQ_TY3VYJ0NZXTh6woO9pM_M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP501885.RAGK9gzpGGVPWZWnuBUFhHQ_TY3VYJ0NZXTh6woO9pM_M130_assertion
{
miriam-gene:3133
a
ncit:C16612
.
lld:C0678236
a
ncit:C7057
.
dgn-gda:DGN9da776df8690123ae9de504a24af4f5e
sio:SIO_000628
miriam-gene:3133
,
lld:C0678236
;
a
sio:SIO_001121
.
}
dgn-np:NP501885.RAGK9gzpGGVPWZWnuBUFhHQ_TY3VYJ0NZXTh6woO9pM_M130_provenance
{
dgn-np:NP501885.RAGK9gzpGGVPWZWnuBUFhHQ_TY3VYJ0NZXTh6woO9pM_M130_assertion
dcterms:description
"[There are at least four complementation groups and the genetic and molecular dissection of this rare disease has contributed considerably to our current understanding of the molecular mechanisms governing MHC class II expression.]. 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:9099848
;
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:NP501885.RAGK9gzpGGVPWZWnuBUFhHQ_TY3VYJ0NZXTh6woO9pM_M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:59+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" .
}