@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP611060.RA7Q2UD655ZBe87vFIaztW0RPAtHhGH5xUKg-asrAQhuQ
> .
@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:NP611060.RA7Q2UD655ZBe87vFIaztW0RPAtHhGH5xUKg-asrAQhuQ130_head
{
this:
np:hasAssertion
dgn-np:NP611060.RA7Q2UD655ZBe87vFIaztW0RPAtHhGH5xUKg-asrAQhuQ130_assertion
;
np:hasProvenance
dgn-np:NP611060.RA7Q2UD655ZBe87vFIaztW0RPAtHhGH5xUKg-asrAQhuQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP611060.RA7Q2UD655ZBe87vFIaztW0RPAtHhGH5xUKg-asrAQhuQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP611060.RA7Q2UD655ZBe87vFIaztW0RPAtHhGH5xUKg-asrAQhuQ130_assertion
a
np:Assertion
.
dgn-np:NP611060.RA7Q2UD655ZBe87vFIaztW0RPAtHhGH5xUKg-asrAQhuQ130_provenance
a
np:Provenance
.
dgn-np:NP611060.RA7Q2UD655ZBe87vFIaztW0RPAtHhGH5xUKg-asrAQhuQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP611060.RA7Q2UD655ZBe87vFIaztW0RPAtHhGH5xUKg-asrAQhuQ130_assertion
{
miriam-gene:1861
a
ncit:C16612
.
lld:C0018213
a
ncit:C7057
.
dgn-gda:DGN1c768068276c7ecb0ff6e80fb6d059a1
sio:SIO_000628
miriam-gene:1861
,
lld:C0018213
;
a
sio:SIO_001121
.
}
dgn-np:NP611060.RA7Q2UD655ZBe87vFIaztW0RPAtHhGH5xUKg-asrAQhuQ130_provenance
{
dgn-np:NP611060.RA7Q2UD655ZBe87vFIaztW0RPAtHhGH5xUKg-asrAQhuQ130_assertion
dcterms:description
"[Furthermore the transmission analysis in GD and HT families revealed no differences in alleles transmission for rs1990760 IFIH1 from parents with or without HLA risk haplotype DQ2 to the affected offspring.]. 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:19961590
;
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:NP611060.RA7Q2UD655ZBe87vFIaztW0RPAtHhGH5xUKg-asrAQhuQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:09+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" .
}