@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP343971.RAOOP1gNgRT_QpRfe0ygbjK4ZV6h4rAM0_ftTLqNWUIjc
> .
@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/v4.0.0/void/
> .
dgn-np:NP343971.RAOOP1gNgRT_QpRfe0ygbjK4ZV6h4rAM0_ftTLqNWUIjc130_head
{
this:
np:hasAssertion
dgn-np:NP343971.RAOOP1gNgRT_QpRfe0ygbjK4ZV6h4rAM0_ftTLqNWUIjc130_assertion
;
np:hasProvenance
dgn-np:NP343971.RAOOP1gNgRT_QpRfe0ygbjK4ZV6h4rAM0_ftTLqNWUIjc130_provenance
;
np:hasPublicationInfo
dgn-np:NP343971.RAOOP1gNgRT_QpRfe0ygbjK4ZV6h4rAM0_ftTLqNWUIjc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP343971.RAOOP1gNgRT_QpRfe0ygbjK4ZV6h4rAM0_ftTLqNWUIjc130_assertion
a
np:Assertion
.
dgn-np:NP343971.RAOOP1gNgRT_QpRfe0ygbjK4ZV6h4rAM0_ftTLqNWUIjc130_provenance
a
np:Provenance
.
dgn-np:NP343971.RAOOP1gNgRT_QpRfe0ygbjK4ZV6h4rAM0_ftTLqNWUIjc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP343971.RAOOP1gNgRT_QpRfe0ygbjK4ZV6h4rAM0_ftTLqNWUIjc130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C0596263
a
ncit:C7057
.
dgn-gda:DGN43c160c73b0b08e8e16763c0b39e969c
sio:SIO_000628
miriam-gene:7248
,
lld:C0596263
;
a
sio:SIO_001121
.
}
dgn-np:NP343971.RAOOP1gNgRT_QpRfe0ygbjK4ZV6h4rAM0_ftTLqNWUIjc130_provenance
{
dgn-np:NP343971.RAOOP1gNgRT_QpRfe0ygbjK4ZV6h4rAM0_ftTLqNWUIjc130_assertion
dcterms:description
"[Inactivation of both copies of a tumour suppressor gene is required for carcinogenesis, while germline deletion or inactivation of one copy results in an increase in the risk of cancer and is responsible for many of the known hereditary cancer syndromes.]. 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:11826018
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP343971.RAOOP1gNgRT_QpRfe0ygbjK4ZV6h4rAM0_ftTLqNWUIjc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:21+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}