@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP832615.RAqXreoMmpCGq3Pz5rO4octpBKij1CEM6BMuANg7eHvLA
> .
@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:NP832615.RAqXreoMmpCGq3Pz5rO4octpBKij1CEM6BMuANg7eHvLA130_head
{
this:
np:hasAssertion
dgn-np:NP832615.RAqXreoMmpCGq3Pz5rO4octpBKij1CEM6BMuANg7eHvLA130_assertion
;
np:hasProvenance
dgn-np:NP832615.RAqXreoMmpCGq3Pz5rO4octpBKij1CEM6BMuANg7eHvLA130_provenance
;
np:hasPublicationInfo
dgn-np:NP832615.RAqXreoMmpCGq3Pz5rO4octpBKij1CEM6BMuANg7eHvLA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP832615.RAqXreoMmpCGq3Pz5rO4octpBKij1CEM6BMuANg7eHvLA130_assertion
a
np:Assertion
.
dgn-np:NP832615.RAqXreoMmpCGq3Pz5rO4octpBKij1CEM6BMuANg7eHvLA130_provenance
a
np:Provenance
.
dgn-np:NP832615.RAqXreoMmpCGq3Pz5rO4octpBKij1CEM6BMuANg7eHvLA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP832615.RAqXreoMmpCGq3Pz5rO4octpBKij1CEM6BMuANg7eHvLA130_assertion
{
miriam-gene:27242
a
ncit:C16612
.
lld:C0011849
a
ncit:C7057
.
dgn-gda:DGN5fcbc1f60a3c2361e0e0f268048fdf72
sio:SIO_000628
miriam-gene:27242
,
lld:C0011849
;
a
sio:SIO_001121
.
}
dgn-np:NP832615.RAqXreoMmpCGq3Pz5rO4octpBKij1CEM6BMuANg7eHvLA130_provenance
{
dgn-np:NP832615.RAqXreoMmpCGq3Pz5rO4octpBKij1CEM6BMuANg7eHvLA130_assertion
dcterms:description
"[HLA typing of the family members showed that the diabetes was probably associated with an HLA AW30, BW38, DR4 haplotype, found in both sisters and in their father, and that the thyroid disease was associated with the A29, B7, DR6 haplotype found in the patient and in her mother.]. 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:6511337
;
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:NP832615.RAqXreoMmpCGq3Pz5rO4octpBKij1CEM6BMuANg7eHvLA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:29+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" .
}