@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP509661.RAxqlVENwIfn4UVucKP0uADYS9haX3OtWRyHpkzKgDsjI
> .
@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:NP509661.RAxqlVENwIfn4UVucKP0uADYS9haX3OtWRyHpkzKgDsjI130_head
{
this:
np:hasAssertion
dgn-np:NP509661.RAxqlVENwIfn4UVucKP0uADYS9haX3OtWRyHpkzKgDsjI130_assertion
;
np:hasProvenance
dgn-np:NP509661.RAxqlVENwIfn4UVucKP0uADYS9haX3OtWRyHpkzKgDsjI130_provenance
;
np:hasPublicationInfo
dgn-np:NP509661.RAxqlVENwIfn4UVucKP0uADYS9haX3OtWRyHpkzKgDsjI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP509661.RAxqlVENwIfn4UVucKP0uADYS9haX3OtWRyHpkzKgDsjI130_assertion
a
np:Assertion
.
dgn-np:NP509661.RAxqlVENwIfn4UVucKP0uADYS9haX3OtWRyHpkzKgDsjI130_provenance
a
np:Provenance
.
dgn-np:NP509661.RAxqlVENwIfn4UVucKP0uADYS9haX3OtWRyHpkzKgDsjI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP509661.RAxqlVENwIfn4UVucKP0uADYS9haX3OtWRyHpkzKgDsjI130_assertion
{
miriam-gene:64135
a
ncit:C16612
.
lld:C0011854
a
ncit:C7057
.
dgn-gda:DGNd2ed524b71ceb24984003d71cbab74b2
sio:SIO_000628
miriam-gene:64135
,
lld:C0011854
;
a
sio:SIO_001121
.
}
dgn-np:NP509661.RAxqlVENwIfn4UVucKP0uADYS9haX3OtWRyHpkzKgDsjI130_provenance
{
dgn-np:NP509661.RAxqlVENwIfn4UVucKP0uADYS9haX3OtWRyHpkzKgDsjI130_assertion
dcterms:description
"[Moreover, the association of the Thr946Ala SNP with T1D is not due to modulation of IFIH1 expression in organs involved in the disease, pointing to the IFIH1 nsSNP as the causal variant.]. 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:20644636
;
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:NP509661.RAxqlVENwIfn4UVucKP0uADYS9haX3OtWRyHpkzKgDsjI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:04+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" .
}