@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP419747.RAw5jEYhR6SCHtV70llYfn97XVHptF0wF4_7s61L2XF_Q
> .
@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:NP419747.RAw5jEYhR6SCHtV70llYfn97XVHptF0wF4_7s61L2XF_Q130_head
{
this:
np:hasAssertion
dgn-np:NP419747.RAw5jEYhR6SCHtV70llYfn97XVHptF0wF4_7s61L2XF_Q130_assertion
;
np:hasProvenance
dgn-np:NP419747.RAw5jEYhR6SCHtV70llYfn97XVHptF0wF4_7s61L2XF_Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP419747.RAw5jEYhR6SCHtV70llYfn97XVHptF0wF4_7s61L2XF_Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP419747.RAw5jEYhR6SCHtV70llYfn97XVHptF0wF4_7s61L2XF_Q130_assertion
a
np:Assertion
.
dgn-np:NP419747.RAw5jEYhR6SCHtV70llYfn97XVHptF0wF4_7s61L2XF_Q130_provenance
a
np:Provenance
.
dgn-np:NP419747.RAw5jEYhR6SCHtV70llYfn97XVHptF0wF4_7s61L2XF_Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP419747.RAw5jEYhR6SCHtV70llYfn97XVHptF0wF4_7s61L2XF_Q130_assertion
{
miriam-gene:57498
a
ncit:C16612
.
lld:C0011854
a
ncit:C7057
.
dgn-gda:DGN0e5abee4c95a18b8344320a36d86f211
sio:SIO_000628
miriam-gene:57498
,
lld:C0011854
;
a
sio:SIO_001121
.
}
dgn-np:NP419747.RAw5jEYhR6SCHtV70llYfn97XVHptF0wF4_7s61L2XF_Q130_provenance
{
dgn-np:NP419747.RAw5jEYhR6SCHtV70llYfn97XVHptF0wF4_7s61L2XF_Q130_assertion
dcterms:description
"[Since polymorphisms of TAP might influence susceptibility to IDDM possibly by selection of different antigen peptides, we investigated sequence variants of TAP1 and TAP2 genes in 120 German patients with IDDM and 218 random healthy German controls by polymerase chain reaction (PCR) followed by sequence-specific oligonucleotide analysis (SSO), single-strand conformation 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:9226129
;
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:NP419747.RAw5jEYhR6SCHtV70llYfn97XVHptF0wF4_7s61L2XF_Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:09+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" .
}