@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP759152.RAkTiLc5HuFyvNAySqDUsxkzOyyh2QF9xQXa7EqsCEPkA
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP759152.RAkTiLc5HuFyvNAySqDUsxkzOyyh2QF9xQXa7EqsCEPkA130_head
{
this:
np:hasAssertion
dgn-np:NP759152.RAkTiLc5HuFyvNAySqDUsxkzOyyh2QF9xQXa7EqsCEPkA130_assertion
;
np:hasProvenance
dgn-np:NP759152.RAkTiLc5HuFyvNAySqDUsxkzOyyh2QF9xQXa7EqsCEPkA130_provenance
;
np:hasPublicationInfo
dgn-np:NP759152.RAkTiLc5HuFyvNAySqDUsxkzOyyh2QF9xQXa7EqsCEPkA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP759152.RAkTiLc5HuFyvNAySqDUsxkzOyyh2QF9xQXa7EqsCEPkA130_assertion
a
np:Assertion
.
dgn-np:NP759152.RAkTiLc5HuFyvNAySqDUsxkzOyyh2QF9xQXa7EqsCEPkA130_provenance
a
np:Provenance
.
dgn-np:NP759152.RAkTiLc5HuFyvNAySqDUsxkzOyyh2QF9xQXa7EqsCEPkA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP759152.RAkTiLc5HuFyvNAySqDUsxkzOyyh2QF9xQXa7EqsCEPkA130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C0032002
a
ncit:C7057
.
dgn-gda:DGNebbb006839379e16e73c84463eb1b537
sio:SIO_000628
miriam-gene:7248
,
lld:C0032002
;
a
sio:SIO_001124
.
}
dgn-np:NP759152.RAkTiLc5HuFyvNAySqDUsxkzOyyh2QF9xQXa7EqsCEPkA130_provenance
{
dgn-np:NP759152.RAkTiLc5HuFyvNAySqDUsxkzOyyh2QF9xQXa7EqsCEPkA130_assertion
dcterms:description
"[Bringing together the data of several groups now allows a tentative map to be drawn showing loss of heterozygosity at several chromosomal loci to be associated with the transition to the invasive and malignant phenotype, while changes associated with chromosome 9p and silencing, through methylation, of the tumour suppressor gene p16 appear to occur early in pituitary tumourigenesis.]. 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:9667798
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP759152.RAkTiLc5HuFyvNAySqDUsxkzOyyh2QF9xQXa7EqsCEPkA130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:18+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}