@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP219937.RAbAueQKVF11RL6rufx0qinuxRQ-i1eKe4JmHUjJegpu0
> .
@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:NP219937.RAbAueQKVF11RL6rufx0qinuxRQ-i1eKe4JmHUjJegpu0130_head
{
this:
np:hasAssertion
dgn-np:NP219937.RAbAueQKVF11RL6rufx0qinuxRQ-i1eKe4JmHUjJegpu0130_assertion
;
np:hasProvenance
dgn-np:NP219937.RAbAueQKVF11RL6rufx0qinuxRQ-i1eKe4JmHUjJegpu0130_provenance
;
np:hasPublicationInfo
dgn-np:NP219937.RAbAueQKVF11RL6rufx0qinuxRQ-i1eKe4JmHUjJegpu0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP219937.RAbAueQKVF11RL6rufx0qinuxRQ-i1eKe4JmHUjJegpu0130_assertion
a
np:Assertion
.
dgn-np:NP219937.RAbAueQKVF11RL6rufx0qinuxRQ-i1eKe4JmHUjJegpu0130_provenance
a
np:Provenance
.
dgn-np:NP219937.RAbAueQKVF11RL6rufx0qinuxRQ-i1eKe4JmHUjJegpu0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP219937.RAbAueQKVF11RL6rufx0qinuxRQ-i1eKe4JmHUjJegpu0130_assertion
{
miriam-gene:3133
a
ncit:C16612
.
lld:C0007570
a
ncit:C7057
.
dgn-gda:DGN4b55f4f284b642f3bb69ad4fcd75d08d
sio:SIO_000628
miriam-gene:3133
,
lld:C0007570
;
a
sio:SIO_001121
.
}
dgn-np:NP219937.RAbAueQKVF11RL6rufx0qinuxRQ-i1eKe4JmHUjJegpu0130_provenance
{
dgn-np:NP219937.RAbAueQKVF11RL6rufx0qinuxRQ-i1eKe4JmHUjJegpu0130_assertion
dcterms:description
"[We have previously shown that the HLA alleles and CD do not co-segregate in families multiply affected with CD, suggesting that the HLA association is entirely due to the necessity to have these normal DQ alleles for CD to manifest, and that the main genetic predisposition lies at a locus other than the MHC.]. 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:9659975
;
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:NP219937.RAbAueQKVF11RL6rufx0qinuxRQ-i1eKe4JmHUjJegpu0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:02+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" .
}