@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP607021.RAjNFSeyxOSwCAXnXcuOgk_VXrEHDbrcJi3-l5YKmTXUY
> .
@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:NP607021.RAjNFSeyxOSwCAXnXcuOgk_VXrEHDbrcJi3-l5YKmTXUY130_head
{
this:
np:hasAssertion
dgn-np:NP607021.RAjNFSeyxOSwCAXnXcuOgk_VXrEHDbrcJi3-l5YKmTXUY130_assertion
;
np:hasProvenance
dgn-np:NP607021.RAjNFSeyxOSwCAXnXcuOgk_VXrEHDbrcJi3-l5YKmTXUY130_provenance
;
np:hasPublicationInfo
dgn-np:NP607021.RAjNFSeyxOSwCAXnXcuOgk_VXrEHDbrcJi3-l5YKmTXUY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP607021.RAjNFSeyxOSwCAXnXcuOgk_VXrEHDbrcJi3-l5YKmTXUY130_assertion
a
np:Assertion
.
dgn-np:NP607021.RAjNFSeyxOSwCAXnXcuOgk_VXrEHDbrcJi3-l5YKmTXUY130_provenance
a
np:Provenance
.
dgn-np:NP607021.RAjNFSeyxOSwCAXnXcuOgk_VXrEHDbrcJi3-l5YKmTXUY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP607021.RAjNFSeyxOSwCAXnXcuOgk_VXrEHDbrcJi3-l5YKmTXUY130_assertion
{
miriam-gene:3126
a
ncit:C16612
.
lld:C0040128
a
ncit:C7057
.
dgn-gda:DGN0c15dbbbd03bc10c1bfc8aa138d20fe1
sio:SIO_000628
miriam-gene:3126
,
lld:C0040128
;
a
sio:SIO_001121
.
}
dgn-np:NP607021.RAjNFSeyxOSwCAXnXcuOgk_VXrEHDbrcJi3-l5YKmTXUY130_provenance
{
dgn-np:NP607021.RAjNFSeyxOSwCAXnXcuOgk_VXrEHDbrcJi3-l5YKmTXUY130_assertion
dcterms:description
"[A total of 80 Kuwaiti children with alopecia areata (AA), without clinical evidence of thyroid disease, were screened for the presence of thyroid abnormalities, and 50 unrelated children with AA were tissue typed for human leukocyte antigen (HLA) class I and class II antigens.]. 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:12437547
;
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:NP607021.RAjNFSeyxOSwCAXnXcuOgk_VXrEHDbrcJi3-l5YKmTXUY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:04+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" .
}