@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP246647.RADYTmFecC7StjnCKnYVYcPxVqjSdL-uK_FKyf7OWQ3YY
> .
@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:NP246647.RADYTmFecC7StjnCKnYVYcPxVqjSdL-uK_FKyf7OWQ3YY130_head
{
this:
np:hasAssertion
dgn-np:NP246647.RADYTmFecC7StjnCKnYVYcPxVqjSdL-uK_FKyf7OWQ3YY130_assertion
;
np:hasProvenance
dgn-np:NP246647.RADYTmFecC7StjnCKnYVYcPxVqjSdL-uK_FKyf7OWQ3YY130_provenance
;
np:hasPublicationInfo
dgn-np:NP246647.RADYTmFecC7StjnCKnYVYcPxVqjSdL-uK_FKyf7OWQ3YY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP246647.RADYTmFecC7StjnCKnYVYcPxVqjSdL-uK_FKyf7OWQ3YY130_assertion
a
np:Assertion
.
dgn-np:NP246647.RADYTmFecC7StjnCKnYVYcPxVqjSdL-uK_FKyf7OWQ3YY130_provenance
a
np:Provenance
.
dgn-np:NP246647.RADYTmFecC7StjnCKnYVYcPxVqjSdL-uK_FKyf7OWQ3YY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP246647.RADYTmFecC7StjnCKnYVYcPxVqjSdL-uK_FKyf7OWQ3YY130_assertion
{
miriam-gene:3126
a
ncit:C16612
.
lld:C0007570
a
ncit:C7057
.
dgn-gda:DGN649d29393a2678e8974a0771bb3c8d6c
sio:SIO_000628
miriam-gene:3126
,
lld:C0007570
;
a
sio:SIO_001121
.
}
dgn-np:NP246647.RADYTmFecC7StjnCKnYVYcPxVqjSdL-uK_FKyf7OWQ3YY130_provenance
{
dgn-np:NP246647.RADYTmFecC7StjnCKnYVYcPxVqjSdL-uK_FKyf7OWQ3YY130_assertion
dcterms:description
"[The need for an early and accurate diagnosis in celiac disease (CD) has focused attention on new diagnostic approaches, based on the efficiency of serological markers and the high negative predictive value of human leukocyte antigen (HLA) non-DQ2/8.]. 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:23111763
;
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:NP246647.RADYTmFecC7StjnCKnYVYcPxVqjSdL-uK_FKyf7OWQ3YY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:18+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" .
}