@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP445101.RA6O5tnSeoCtMDUad8Q2sagtrQmQ_R9BRhBFargF-HrK0
> .
@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:NP445101.RA6O5tnSeoCtMDUad8Q2sagtrQmQ_R9BRhBFargF-HrK0130_head
{
this:
np:hasAssertion
dgn-np:NP445101.RA6O5tnSeoCtMDUad8Q2sagtrQmQ_R9BRhBFargF-HrK0130_assertion
;
np:hasProvenance
dgn-np:NP445101.RA6O5tnSeoCtMDUad8Q2sagtrQmQ_R9BRhBFargF-HrK0130_provenance
;
np:hasPublicationInfo
dgn-np:NP445101.RA6O5tnSeoCtMDUad8Q2sagtrQmQ_R9BRhBFargF-HrK0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP445101.RA6O5tnSeoCtMDUad8Q2sagtrQmQ_R9BRhBFargF-HrK0130_assertion
a
np:Assertion
.
dgn-np:NP445101.RA6O5tnSeoCtMDUad8Q2sagtrQmQ_R9BRhBFargF-HrK0130_provenance
a
np:Provenance
.
dgn-np:NP445101.RA6O5tnSeoCtMDUad8Q2sagtrQmQ_R9BRhBFargF-HrK0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP445101.RA6O5tnSeoCtMDUad8Q2sagtrQmQ_R9BRhBFargF-HrK0130_assertion
{
miriam-gene:7251
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNf93fa427b9d43ac9acb497133fa40865
sio:SIO_000628
miriam-gene:7251
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP445101.RA6O5tnSeoCtMDUad8Q2sagtrQmQ_R9BRhBFargF-HrK0130_provenance
{
dgn-np:NP445101.RA6O5tnSeoCtMDUad8Q2sagtrQmQ_R9BRhBFargF-HrK0130_assertion
dcterms:description
"[Truncated TSG101 transcripts that probably represent splice variants are present in some breast and ovarian cancers, but there is no evidence to suggest that loss of this putative tumor suppressor gene plays a role in the molecular pathogenesis of these cancers.]. 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:9773405
;
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:NP445101.RA6O5tnSeoCtMDUad8Q2sagtrQmQ_R9BRhBFargF-HrK0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:25+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" .
}