@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP937393.RA2hLOkV8YU_lmcBpTGYcSHemUzsiciiXB9YFa5l7prI8
> .
@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:NP937393.RA2hLOkV8YU_lmcBpTGYcSHemUzsiciiXB9YFa5l7prI8130_head
{
this:
np:hasAssertion
dgn-np:NP937393.RA2hLOkV8YU_lmcBpTGYcSHemUzsiciiXB9YFa5l7prI8130_assertion
;
np:hasProvenance
dgn-np:NP937393.RA2hLOkV8YU_lmcBpTGYcSHemUzsiciiXB9YFa5l7prI8130_provenance
;
np:hasPublicationInfo
dgn-np:NP937393.RA2hLOkV8YU_lmcBpTGYcSHemUzsiciiXB9YFa5l7prI8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP937393.RA2hLOkV8YU_lmcBpTGYcSHemUzsiciiXB9YFa5l7prI8130_assertion
a
np:Assertion
.
dgn-np:NP937393.RA2hLOkV8YU_lmcBpTGYcSHemUzsiciiXB9YFa5l7prI8130_provenance
a
np:Provenance
.
dgn-np:NP937393.RA2hLOkV8YU_lmcBpTGYcSHemUzsiciiXB9YFa5l7prI8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP937393.RA2hLOkV8YU_lmcBpTGYcSHemUzsiciiXB9YFa5l7prI8130_assertion
{
miriam-gene:1950
a
ncit:C16612
.
lld:C0027708
a
ncit:C7057
.
dgn-gda:DGNafcc0e84bc681fc9251a61b97635329f
sio:SIO_000628
miriam-gene:1950
,
lld:C0027708
;
a
sio:SIO_001121
.
}
dgn-np:NP937393.RA2hLOkV8YU_lmcBpTGYcSHemUzsiciiXB9YFa5l7prI8130_provenance
{
dgn-np:NP937393.RA2hLOkV8YU_lmcBpTGYcSHemUzsiciiXB9YFa5l7prI8130_assertion
dcterms:description
"[We demonstrate that WT1 could normally serve to suppress EGF receptor expression in VGEC, since immunoreactive EGF receptor is strikingly absent compared to epithelial cells of the emerging proximal and distal tubule, which lack WT1.]. 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:9291179
;
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:NP937393.RA2hLOkV8YU_lmcBpTGYcSHemUzsiciiXB9YFa5l7prI8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:34+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" .
}