@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP586688.RAaA3wkGShLX7RpsqBQJaSlsDB6AIKlqICv5Sos5xGwPo
> .
@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:NP586688.RAaA3wkGShLX7RpsqBQJaSlsDB6AIKlqICv5Sos5xGwPo130_head
{
this:
np:hasAssertion
dgn-np:NP586688.RAaA3wkGShLX7RpsqBQJaSlsDB6AIKlqICv5Sos5xGwPo130_assertion
;
np:hasProvenance
dgn-np:NP586688.RAaA3wkGShLX7RpsqBQJaSlsDB6AIKlqICv5Sos5xGwPo130_provenance
;
np:hasPublicationInfo
dgn-np:NP586688.RAaA3wkGShLX7RpsqBQJaSlsDB6AIKlqICv5Sos5xGwPo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP586688.RAaA3wkGShLX7RpsqBQJaSlsDB6AIKlqICv5Sos5xGwPo130_assertion
a
np:Assertion
.
dgn-np:NP586688.RAaA3wkGShLX7RpsqBQJaSlsDB6AIKlqICv5Sos5xGwPo130_provenance
a
np:Provenance
.
dgn-np:NP586688.RAaA3wkGShLX7RpsqBQJaSlsDB6AIKlqICv5Sos5xGwPo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP586688.RAaA3wkGShLX7RpsqBQJaSlsDB6AIKlqICv5Sos5xGwPo130_assertion
{
miriam-gene:3133
a
ncit:C16612
.
lld:C0011608
a
ncit:C7057
.
dgn-gda:DGN4e1e42193e46dc4248879c91dad2f29a
sio:SIO_000628
miriam-gene:3133
,
lld:C0011608
;
a
sio:SIO_001121
.
}
dgn-np:NP586688.RAaA3wkGShLX7RpsqBQJaSlsDB6AIKlqICv5Sos5xGwPo130_provenance
{
dgn-np:NP586688.RAaA3wkGShLX7RpsqBQJaSlsDB6AIKlqICv5Sos5xGwPo130_assertion
dcterms:description
"[These findings suggest that the MHC susceptibility gene for DH is between class II and complotype regions, closest to the complotype, whereas that for GSE is in the class II region.]. 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:8245782
;
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:NP586688.RAaA3wkGShLX7RpsqBQJaSlsDB6AIKlqICv5Sos5xGwPo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:53+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" .
}