@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP770514.RA76Y0744V_QSV3JycxuVv08RA9SUF_UQaEVsUk3CzHRo
> .
@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:NP770514.RA76Y0744V_QSV3JycxuVv08RA9SUF_UQaEVsUk3CzHRo130_head
{
this:
np:hasAssertion
dgn-np:NP770514.RA76Y0744V_QSV3JycxuVv08RA9SUF_UQaEVsUk3CzHRo130_assertion
;
np:hasProvenance
dgn-np:NP770514.RA76Y0744V_QSV3JycxuVv08RA9SUF_UQaEVsUk3CzHRo130_provenance
;
np:hasPublicationInfo
dgn-np:NP770514.RA76Y0744V_QSV3JycxuVv08RA9SUF_UQaEVsUk3CzHRo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP770514.RA76Y0744V_QSV3JycxuVv08RA9SUF_UQaEVsUk3CzHRo130_assertion
a
np:Assertion
.
dgn-np:NP770514.RA76Y0744V_QSV3JycxuVv08RA9SUF_UQaEVsUk3CzHRo130_provenance
a
np:Provenance
.
dgn-np:NP770514.RA76Y0744V_QSV3JycxuVv08RA9SUF_UQaEVsUk3CzHRo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP770514.RA76Y0744V_QSV3JycxuVv08RA9SUF_UQaEVsUk3CzHRo130_assertion
{
miriam-gene:3105
a
ncit:C16612
.
lld:C0026896
a
ncit:C7057
.
dgn-gda:DGNabfa2d7ff8da2b9f8f97ff098ea10158
sio:SIO_000628
miriam-gene:3105
,
lld:C0026896
;
a
sio:SIO_001121
.
}
dgn-np:NP770514.RA76Y0744V_QSV3JycxuVv08RA9SUF_UQaEVsUk3CzHRo130_provenance
{
dgn-np:NP770514.RA76Y0744V_QSV3JycxuVv08RA9SUF_UQaEVsUk3CzHRo130_assertion
dcterms:description
"[Using the technique of in vitro enzymatic DNA amplification and dot blot hybridization with sequence-specific oligonucleotide (SSO) probes, a study of genetic polymorphism of HLA-DPB1 was performed in 83 unrelated patients with Graves' disease (GD), 48 patients with early onset myasthenia gravis (EOMG) and 100 normal British caucasoid subjects who were also tissue typed for HLA-A, B and DR 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:8061167
;
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:NP770514.RA76Y0744V_QSV3JycxuVv08RA9SUF_UQaEVsUk3CzHRo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:46+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" .
}