@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP224060.RAde2YnWRiBM1EnYWidkhO7vaY1tf5wcEPF8sGt6H4fwA
> .
@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:NP224060.RAde2YnWRiBM1EnYWidkhO7vaY1tf5wcEPF8sGt6H4fwA130_head
{
this:
np:hasAssertion
dgn-np:NP224060.RAde2YnWRiBM1EnYWidkhO7vaY1tf5wcEPF8sGt6H4fwA130_assertion
;
np:hasProvenance
dgn-np:NP224060.RAde2YnWRiBM1EnYWidkhO7vaY1tf5wcEPF8sGt6H4fwA130_provenance
;
np:hasPublicationInfo
dgn-np:NP224060.RAde2YnWRiBM1EnYWidkhO7vaY1tf5wcEPF8sGt6H4fwA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP224060.RAde2YnWRiBM1EnYWidkhO7vaY1tf5wcEPF8sGt6H4fwA130_assertion
a
np:Assertion
.
dgn-np:NP224060.RAde2YnWRiBM1EnYWidkhO7vaY1tf5wcEPF8sGt6H4fwA130_provenance
a
np:Provenance
.
dgn-np:NP224060.RAde2YnWRiBM1EnYWidkhO7vaY1tf5wcEPF8sGt6H4fwA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP224060.RAde2YnWRiBM1EnYWidkhO7vaY1tf5wcEPF8sGt6H4fwA130_assertion
{
miriam-gene:6344
a
ncit:C16612
.
lld:C0031511
a
ncit:C7057
.
dgn-gda:DGNde5a189873dc75c96c54b8b3a872d39c
sio:SIO_000628
miriam-gene:6344
,
lld:C0031511
;
a
sio:SIO_001121
.
}
dgn-np:NP224060.RAde2YnWRiBM1EnYWidkhO7vaY1tf5wcEPF8sGt6H4fwA130_provenance
{
dgn-np:NP224060.RAde2YnWRiBM1EnYWidkhO7vaY1tf5wcEPF8sGt6H4fwA130_assertion
dcterms:description
"[We recently discovered that pheochromocytomas developing in rats affected by the MENX (multiple endocrine neoplasia-like) syndrome express at very high-level Sctr, encoding SR. We here report that SR are also highly abundant on the membranes of rat adrenal and extraadrenal pheochromocytoma, starting from early stages of tumor development, and are functional.]. 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:22692904
;
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:NP224060.RAde2YnWRiBM1EnYWidkhO7vaY1tf5wcEPF8sGt6H4fwA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:04+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" .
}