@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP698423.RATBSzdI30z_P0XCTRv4hl1G6pRB_1wQSlQzJ98Jcnrws
> .
@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:NP698423.RATBSzdI30z_P0XCTRv4hl1G6pRB_1wQSlQzJ98Jcnrws130_head
{
this:
np:hasAssertion
dgn-np:NP698423.RATBSzdI30z_P0XCTRv4hl1G6pRB_1wQSlQzJ98Jcnrws130_assertion
;
np:hasProvenance
dgn-np:NP698423.RATBSzdI30z_P0XCTRv4hl1G6pRB_1wQSlQzJ98Jcnrws130_provenance
;
np:hasPublicationInfo
dgn-np:NP698423.RATBSzdI30z_P0XCTRv4hl1G6pRB_1wQSlQzJ98Jcnrws130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP698423.RATBSzdI30z_P0XCTRv4hl1G6pRB_1wQSlQzJ98Jcnrws130_assertion
a
np:Assertion
.
dgn-np:NP698423.RATBSzdI30z_P0XCTRv4hl1G6pRB_1wQSlQzJ98Jcnrws130_provenance
a
np:Provenance
.
dgn-np:NP698423.RATBSzdI30z_P0XCTRv4hl1G6pRB_1wQSlQzJ98Jcnrws130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP698423.RATBSzdI30z_P0XCTRv4hl1G6pRB_1wQSlQzJ98Jcnrws130_assertion
{
miriam-gene:57498
a
ncit:C16612
.
lld:C0018213
a
ncit:C7057
.
dgn-gda:DGN6f56b2bf15a30db67959e20cb1f307db
sio:SIO_000628
miriam-gene:57498
,
lld:C0018213
;
a
sio:SIO_001121
.
}
dgn-np:NP698423.RATBSzdI30z_P0XCTRv4hl1G6pRB_1wQSlQzJ98Jcnrws130_provenance
{
dgn-np:NP698423.RATBSzdI30z_P0XCTRv4hl1G6pRB_1wQSlQzJ98Jcnrws130_assertion
dcterms:description
"[Since polymorphisms of TAP might influence susceptibility to Graves' disease by a possibly different selection of antigenic peptides, we investigated sequence variants of TAP1 and TAP2 genes in 235 patients with Graves' disease and 218 random healthy controls by polymerase chain reaction (PCR) followed by sequence specific oligonucleotide analysis (SSO), single strand conformational polymorphism (SSCP) analysis and amplification refractory mutation system (ARMS).]. 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:9027960
;
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:NP698423.RATBSzdI30z_P0XCTRv4hl1G6pRB_1wQSlQzJ98Jcnrws130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:04+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" .
}