@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP816448.RApNFgr4CLzs2POrSyeotsvUtfcZgZQ8dFx7lOx45kmyw
> .
@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:NP816448.RApNFgr4CLzs2POrSyeotsvUtfcZgZQ8dFx7lOx45kmyw130_head
{
this:
np:hasAssertion
dgn-np:NP816448.RApNFgr4CLzs2POrSyeotsvUtfcZgZQ8dFx7lOx45kmyw130_assertion
;
np:hasProvenance
dgn-np:NP816448.RApNFgr4CLzs2POrSyeotsvUtfcZgZQ8dFx7lOx45kmyw130_provenance
;
np:hasPublicationInfo
dgn-np:NP816448.RApNFgr4CLzs2POrSyeotsvUtfcZgZQ8dFx7lOx45kmyw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP816448.RApNFgr4CLzs2POrSyeotsvUtfcZgZQ8dFx7lOx45kmyw130_assertion
a
np:Assertion
.
dgn-np:NP816448.RApNFgr4CLzs2POrSyeotsvUtfcZgZQ8dFx7lOx45kmyw130_provenance
a
np:Provenance
.
dgn-np:NP816448.RApNFgr4CLzs2POrSyeotsvUtfcZgZQ8dFx7lOx45kmyw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP816448.RApNFgr4CLzs2POrSyeotsvUtfcZgZQ8dFx7lOx45kmyw130_assertion
{
miriam-gene:8945
a
ncit:C16612
.
lld:C0025149
a
ncit:C7057
.
dgn-gda:DGNf7dda8d9cd61d6f48ec3fb5f2672af0a
sio:SIO_000628
miriam-gene:8945
,
lld:C0025149
;
a
sio:SIO_001121
.
}
dgn-np:NP816448.RApNFgr4CLzs2POrSyeotsvUtfcZgZQ8dFx7lOx45kmyw130_provenance
{
dgn-np:NP816448.RApNFgr4CLzs2POrSyeotsvUtfcZgZQ8dFx7lOx45kmyw130_assertion
dcterms:description
"[This region contains three genes, MXI1, SUFU and BTRC, which represent putative medulloblastoma tumor suppressor (TS) genes on the basis of either (i) negative regulation of critical medulloblastoma pathways, or (ii) mutation in other cancer types.]. 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:17102621
;
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:NP816448.RApNFgr4CLzs2POrSyeotsvUtfcZgZQ8dFx7lOx45kmyw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:20+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" .
}