@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP736870.RASeOunqf_MxXlJqh9RJlDl2i_Hv6OjJpLRV06GzMIhoY
> .
@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:NP736870.RASeOunqf_MxXlJqh9RJlDl2i_Hv6OjJpLRV06GzMIhoY130_head
{
this:
np:hasAssertion
dgn-np:NP736870.RASeOunqf_MxXlJqh9RJlDl2i_Hv6OjJpLRV06GzMIhoY130_assertion
;
np:hasProvenance
dgn-np:NP736870.RASeOunqf_MxXlJqh9RJlDl2i_Hv6OjJpLRV06GzMIhoY130_provenance
;
np:hasPublicationInfo
dgn-np:NP736870.RASeOunqf_MxXlJqh9RJlDl2i_Hv6OjJpLRV06GzMIhoY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP736870.RASeOunqf_MxXlJqh9RJlDl2i_Hv6OjJpLRV06GzMIhoY130_assertion
a
np:Assertion
.
dgn-np:NP736870.RASeOunqf_MxXlJqh9RJlDl2i_Hv6OjJpLRV06GzMIhoY130_provenance
a
np:Provenance
.
dgn-np:NP736870.RASeOunqf_MxXlJqh9RJlDl2i_Hv6OjJpLRV06GzMIhoY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP736870.RASeOunqf_MxXlJqh9RJlDl2i_Hv6OjJpLRV06GzMIhoY130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0206754
a
ncit:C7057
.
dgn-gda:DGNe4044a253fba75eccabdbae0011fb0c7
sio:SIO_000628
miriam-gene:7157
,
lld:C0206754
;
a
sio:SIO_001121
.
}
dgn-np:NP736870.RASeOunqf_MxXlJqh9RJlDl2i_Hv6OjJpLRV06GzMIhoY130_provenance
{
dgn-np:NP736870.RASeOunqf_MxXlJqh9RJlDl2i_Hv6OjJpLRV06GzMIhoY130_assertion
dcterms:description
"[Since the oncogenic effect of SV40 TAg is caused by inactivation of the tumor suppressor proteins p53 and RB1 and loss of function of these proteins is commonly observed in human neuroendocrine tumors, a similar mechanism might cause neuroendocrine phenotypes in human tumors.]. 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:22253802
;
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:NP736870.RASeOunqf_MxXlJqh9RJlDl2i_Hv6OjJpLRV06GzMIhoY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:27+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" .
}