@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP583236.RA9FZfLfGKhYs84_F1cRxP9h7C90XtwzcmTipyqxeMOXg
> .
@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:NP583236.RA9FZfLfGKhYs84_F1cRxP9h7C90XtwzcmTipyqxeMOXg130_head
{
this:
np:hasAssertion
dgn-np:NP583236.RA9FZfLfGKhYs84_F1cRxP9h7C90XtwzcmTipyqxeMOXg130_assertion
;
np:hasProvenance
dgn-np:NP583236.RA9FZfLfGKhYs84_F1cRxP9h7C90XtwzcmTipyqxeMOXg130_provenance
;
np:hasPublicationInfo
dgn-np:NP583236.RA9FZfLfGKhYs84_F1cRxP9h7C90XtwzcmTipyqxeMOXg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP583236.RA9FZfLfGKhYs84_F1cRxP9h7C90XtwzcmTipyqxeMOXg130_assertion
a
np:Assertion
.
dgn-np:NP583236.RA9FZfLfGKhYs84_F1cRxP9h7C90XtwzcmTipyqxeMOXg130_provenance
a
np:Provenance
.
dgn-np:NP583236.RA9FZfLfGKhYs84_F1cRxP9h7C90XtwzcmTipyqxeMOXg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP583236.RA9FZfLfGKhYs84_F1cRxP9h7C90XtwzcmTipyqxeMOXg130_assertion
{
miriam-gene:5076
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGNd5a74e3b275d71c50964c0387752369f
sio:SIO_000628
miriam-gene:5076
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP583236.RA9FZfLfGKhYs84_F1cRxP9h7C90XtwzcmTipyqxeMOXg130_provenance
{
dgn-np:NP583236.RA9FZfLfGKhYs84_F1cRxP9h7C90XtwzcmTipyqxeMOXg130_assertion
dcterms:description
"[This study addressed (1) the differentiation characteristics of SBTs and (2) the frequency of SCOUTs lacking PAX2 expression in the FTs of patients with SBTs and compared (3) SCOUT morphology and (4) PAX2 expression with SBTs.]. 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:22089527
;
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:NP583236.RA9FZfLfGKhYs84_F1cRxP9h7C90XtwzcmTipyqxeMOXg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:51+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" .
}