@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP878790.RA82opH63oZGaNrHA0gZ90LXGSE9zvkdQfLod40C0Vvq4
> .
@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:NP878790.RA82opH63oZGaNrHA0gZ90LXGSE9zvkdQfLod40C0Vvq4130_head
{
this:
np:hasAssertion
dgn-np:NP878790.RA82opH63oZGaNrHA0gZ90LXGSE9zvkdQfLod40C0Vvq4130_assertion
;
np:hasProvenance
dgn-np:NP878790.RA82opH63oZGaNrHA0gZ90LXGSE9zvkdQfLod40C0Vvq4130_provenance
;
np:hasPublicationInfo
dgn-np:NP878790.RA82opH63oZGaNrHA0gZ90LXGSE9zvkdQfLod40C0Vvq4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP878790.RA82opH63oZGaNrHA0gZ90LXGSE9zvkdQfLod40C0Vvq4130_assertion
a
np:Assertion
.
dgn-np:NP878790.RA82opH63oZGaNrHA0gZ90LXGSE9zvkdQfLod40C0Vvq4130_provenance
a
np:Provenance
.
dgn-np:NP878790.RA82opH63oZGaNrHA0gZ90LXGSE9zvkdQfLod40C0Vvq4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP878790.RA82opH63oZGaNrHA0gZ90LXGSE9zvkdQfLod40C0Vvq4130_assertion
{
miriam-gene:26191
a
ncit:C16612
.
lld:C0011847
a
ncit:C7057
.
dgn-gda:DGN953461c3b29b411d08462cb45a96cb98
sio:SIO_000628
miriam-gene:26191
,
lld:C0011847
;
a
sio:SIO_001121
.
}
dgn-np:NP878790.RA82opH63oZGaNrHA0gZ90LXGSE9zvkdQfLod40C0Vvq4130_provenance
{
dgn-np:NP878790.RA82opH63oZGaNrHA0gZ90LXGSE9zvkdQfLod40C0Vvq4130_assertion
dcterms:description
"[Furthermore, the affected family-based control (AFBAC) association test and the transmission disequilibrium analysis of multiplex families of European descent from the British Diabetes Association (BDA) Warren Repository indicated that the association was stronger in -1123G > C compared to +1858C > T. In conclusion, the type 1 diabetes association with PTPN22 is confirmed, but it cannot be attributed solely to the +1858C > T 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:16470599
;
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:NP878790.RA82opH63oZGaNrHA0gZ90LXGSE9zvkdQfLod40C0Vvq4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:57+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" .
}