@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP179829.RAxqB7IQsalSbOWXkmEqXP0bVHI317xqvOV9N97Vci_tA
> .
@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:NP179829.RAxqB7IQsalSbOWXkmEqXP0bVHI317xqvOV9N97Vci_tA130_head
{
this:
np:hasAssertion
dgn-np:NP179829.RAxqB7IQsalSbOWXkmEqXP0bVHI317xqvOV9N97Vci_tA130_assertion
;
np:hasProvenance
dgn-np:NP179829.RAxqB7IQsalSbOWXkmEqXP0bVHI317xqvOV9N97Vci_tA130_provenance
;
np:hasPublicationInfo
dgn-np:NP179829.RAxqB7IQsalSbOWXkmEqXP0bVHI317xqvOV9N97Vci_tA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP179829.RAxqB7IQsalSbOWXkmEqXP0bVHI317xqvOV9N97Vci_tA130_assertion
a
np:Assertion
.
dgn-np:NP179829.RAxqB7IQsalSbOWXkmEqXP0bVHI317xqvOV9N97Vci_tA130_provenance
a
np:Provenance
.
dgn-np:NP179829.RAxqB7IQsalSbOWXkmEqXP0bVHI317xqvOV9N97Vci_tA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP179829.RAxqB7IQsalSbOWXkmEqXP0bVHI317xqvOV9N97Vci_tA130_assertion
{
miriam-gene:3117
a
ncit:C16612
.
lld:C0850024
a
ncit:C7057
.
dgn-gda:DGN47a000e1f8d013a4de960e5b41e5c7b5
sio:SIO_000628
miriam-gene:3117
,
lld:C0850024
;
a
sio:SIO_001121
.
}
dgn-np:NP179829.RAxqB7IQsalSbOWXkmEqXP0bVHI317xqvOV9N97Vci_tA130_provenance
{
dgn-np:NP179829.RAxqB7IQsalSbOWXkmEqXP0bVHI317xqvOV9N97Vci_tA130_assertion
dcterms:description
"[The characteristic celiac HLA (DQA1 0501 DQB1 0201 heterodimer) was identified in five relatives with positive challenge (including the patient with more severe mucosal atrophy) but was also present in eight relatives with no evidence of gluten sensitivity in the rectal mucosa.]. 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:9260799
;
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:NP179829.RAxqB7IQsalSbOWXkmEqXP0bVHI317xqvOV9N97Vci_tA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:37+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" .
}