@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP708450.RAdkIR2bgm2zU4w_FsS1jrDUZgOC9RmnehbG7Ft6RT340
> .
@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:NP708450.RAdkIR2bgm2zU4w_FsS1jrDUZgOC9RmnehbG7Ft6RT340130_head
{
this:
np:hasAssertion
dgn-np:NP708450.RAdkIR2bgm2zU4w_FsS1jrDUZgOC9RmnehbG7Ft6RT340130_assertion
;
np:hasProvenance
dgn-np:NP708450.RAdkIR2bgm2zU4w_FsS1jrDUZgOC9RmnehbG7Ft6RT340130_provenance
;
np:hasPublicationInfo
dgn-np:NP708450.RAdkIR2bgm2zU4w_FsS1jrDUZgOC9RmnehbG7Ft6RT340130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP708450.RAdkIR2bgm2zU4w_FsS1jrDUZgOC9RmnehbG7Ft6RT340130_assertion
a
np:Assertion
.
dgn-np:NP708450.RAdkIR2bgm2zU4w_FsS1jrDUZgOC9RmnehbG7Ft6RT340130_provenance
a
np:Provenance
.
dgn-np:NP708450.RAdkIR2bgm2zU4w_FsS1jrDUZgOC9RmnehbG7Ft6RT340130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP708450.RAdkIR2bgm2zU4w_FsS1jrDUZgOC9RmnehbG7Ft6RT340130_assertion
{
miriam-gene:5967
a
ncit:C16612
.
lld:C0011854
a
ncit:C7057
.
dgn-gda:DGNac1ae195ddddae5e567b12b5151b3b03
sio:SIO_000628
miriam-gene:5967
,
lld:C0011854
;
a
sio:SIO_001121
.
}
dgn-np:NP708450.RAdkIR2bgm2zU4w_FsS1jrDUZgOC9RmnehbG7Ft6RT340130_provenance
{
dgn-np:NP708450.RAdkIR2bgm2zU4w_FsS1jrDUZgOC9RmnehbG7Ft6RT340130_assertion
dcterms:description
"[Yet, there are still controversies in the field that require further study and the development of new approaches to extend our understanding of these PTP variants, with the goal of using the information gained to improve our ability to predict and cure T1D.]. 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:23804260
;
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:NP708450.RAdkIR2bgm2zU4w_FsS1jrDUZgOC9RmnehbG7Ft6RT340130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:10+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" .
}