@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP599523.RACaWZYJnnkz3oMfaMtWEhpuiXQlwr_6ZNS319j2Vrjsw
> .
@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:NP599523.RACaWZYJnnkz3oMfaMtWEhpuiXQlwr_6ZNS319j2Vrjsw130_head
{
this:
np:hasAssertion
dgn-np:NP599523.RACaWZYJnnkz3oMfaMtWEhpuiXQlwr_6ZNS319j2Vrjsw130_assertion
;
np:hasProvenance
dgn-np:NP599523.RACaWZYJnnkz3oMfaMtWEhpuiXQlwr_6ZNS319j2Vrjsw130_provenance
;
np:hasPublicationInfo
dgn-np:NP599523.RACaWZYJnnkz3oMfaMtWEhpuiXQlwr_6ZNS319j2Vrjsw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP599523.RACaWZYJnnkz3oMfaMtWEhpuiXQlwr_6ZNS319j2Vrjsw130_assertion
a
np:Assertion
.
dgn-np:NP599523.RACaWZYJnnkz3oMfaMtWEhpuiXQlwr_6ZNS319j2Vrjsw130_provenance
a
np:Provenance
.
dgn-np:NP599523.RACaWZYJnnkz3oMfaMtWEhpuiXQlwr_6ZNS319j2Vrjsw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP599523.RACaWZYJnnkz3oMfaMtWEhpuiXQlwr_6ZNS319j2Vrjsw130_assertion
{
miriam-gene:9223
a
ncit:C16612
.
lld:C0037286
a
ncit:C7057
.
dgn-gda:DGNe3aa1f99eaeed439a209a75e13e0932f
sio:SIO_000628
miriam-gene:9223
,
lld:C0037286
;
a
sio:SIO_001121
.
}
dgn-np:NP599523.RACaWZYJnnkz3oMfaMtWEhpuiXQlwr_6ZNS319j2Vrjsw130_provenance
{
dgn-np:NP599523.RACaWZYJnnkz3oMfaMtWEhpuiXQlwr_6ZNS319j2Vrjsw130_assertion
dcterms:description
"[Recent findings indicate that germline BAP1 mutations cause a novel cancer syndrome that is characterized, at least in the affected families that have been studied so far, by the onset at an early age of benign melanocytic skin tumours with mutated BAP1, and later in life by a high incidence of mesothelioma, uveal melanoma, cutaneous melanoma and possibly additional 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:23550303
;
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:NP599523.RACaWZYJnnkz3oMfaMtWEhpuiXQlwr_6ZNS319j2Vrjsw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:00+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" .
}