@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP720395.RAIlj_4aC0rQi2jRKquzKNNjxleN6hrSYj5eJizNpC74o
> .
@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:NP720395.RAIlj_4aC0rQi2jRKquzKNNjxleN6hrSYj5eJizNpC74o130_head
{
this:
np:hasAssertion
dgn-np:NP720395.RAIlj_4aC0rQi2jRKquzKNNjxleN6hrSYj5eJizNpC74o130_assertion
;
np:hasProvenance
dgn-np:NP720395.RAIlj_4aC0rQi2jRKquzKNNjxleN6hrSYj5eJizNpC74o130_provenance
;
np:hasPublicationInfo
dgn-np:NP720395.RAIlj_4aC0rQi2jRKquzKNNjxleN6hrSYj5eJizNpC74o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP720395.RAIlj_4aC0rQi2jRKquzKNNjxleN6hrSYj5eJizNpC74o130_assertion
a
np:Assertion
.
dgn-np:NP720395.RAIlj_4aC0rQi2jRKquzKNNjxleN6hrSYj5eJizNpC74o130_provenance
a
np:Provenance
.
dgn-np:NP720395.RAIlj_4aC0rQi2jRKquzKNNjxleN6hrSYj5eJizNpC74o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP720395.RAIlj_4aC0rQi2jRKquzKNNjxleN6hrSYj5eJizNpC74o130_assertion
{
miriam-gene:3106
a
ncit:C16612
.
lld:C0007570
a
ncit:C7057
.
dgn-gda:DGNcab057993e0791b870f0361ceba71989
sio:SIO_000628
miriam-gene:3106
,
lld:C0007570
;
a
sio:SIO_001121
.
}
dgn-np:NP720395.RAIlj_4aC0rQi2jRKquzKNNjxleN6hrSYj5eJizNpC74o130_provenance
{
dgn-np:NP720395.RAIlj_4aC0rQi2jRKquzKNNjxleN6hrSYj5eJizNpC74o130_assertion
dcterms:description
"[Although celiac disease has one of the strongest human lymphocyte antigen (HLA) class II associations of any human illness, it is clear that at least one gene that is not linked to the HLA region also is required for its pathogenesis.]. 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:7879822
;
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:NP720395.RAIlj_4aC0rQi2jRKquzKNNjxleN6hrSYj5eJizNpC74o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:17+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" .
}