@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP772760.RA1rtEf-6OxkDeZ54Pc6dFXFpH6cLWGPYkLrcQUy4F8ac
> .
@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:NP772760.RA1rtEf-6OxkDeZ54Pc6dFXFpH6cLWGPYkLrcQUy4F8ac130_head
{
this:
np:hasAssertion
dgn-np:NP772760.RA1rtEf-6OxkDeZ54Pc6dFXFpH6cLWGPYkLrcQUy4F8ac130_assertion
;
np:hasProvenance
dgn-np:NP772760.RA1rtEf-6OxkDeZ54Pc6dFXFpH6cLWGPYkLrcQUy4F8ac130_provenance
;
np:hasPublicationInfo
dgn-np:NP772760.RA1rtEf-6OxkDeZ54Pc6dFXFpH6cLWGPYkLrcQUy4F8ac130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP772760.RA1rtEf-6OxkDeZ54Pc6dFXFpH6cLWGPYkLrcQUy4F8ac130_assertion
a
np:Assertion
.
dgn-np:NP772760.RA1rtEf-6OxkDeZ54Pc6dFXFpH6cLWGPYkLrcQUy4F8ac130_provenance
a
np:Provenance
.
dgn-np:NP772760.RA1rtEf-6OxkDeZ54Pc6dFXFpH6cLWGPYkLrcQUy4F8ac130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP772760.RA1rtEf-6OxkDeZ54Pc6dFXFpH6cLWGPYkLrcQUy4F8ac130_assertion
{
miriam-gene:7857
a
ncit:C16612
.
lld:C0684337
a
ncit:C7057
.
dgn-gda:DGNa3262bd15ee0fcd1a267326977262789
sio:SIO_000628
miriam-gene:7857
,
lld:C0684337
;
a
sio:SIO_001121
.
}
dgn-np:NP772760.RA1rtEf-6OxkDeZ54Pc6dFXFpH6cLWGPYkLrcQUy4F8ac130_provenance
{
dgn-np:NP772760.RA1rtEf-6OxkDeZ54Pc6dFXFpH6cLWGPYkLrcQUy4F8ac130_assertion
dcterms:description
"[Two primary Ewing's sarcomas, one primary PNET (an Askin tumor), and one PNET cell line (TC32) were found to strongly express the SgII gene, as shown by the presence of specific mRNA.]. 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:1342962
;
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:NP772760.RA1rtEf-6OxkDeZ54Pc6dFXFpH6cLWGPYkLrcQUy4F8ac130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:47+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" .
}