@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP588216.RAqUE9bE6r1bSP-o-t3AKh5YKZMQNad29yMEiAMVrqmxg
> .
@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:NP588216.RAqUE9bE6r1bSP-o-t3AKh5YKZMQNad29yMEiAMVrqmxg130_head
{
this:
np:hasAssertion
dgn-np:NP588216.RAqUE9bE6r1bSP-o-t3AKh5YKZMQNad29yMEiAMVrqmxg130_assertion
;
np:hasProvenance
dgn-np:NP588216.RAqUE9bE6r1bSP-o-t3AKh5YKZMQNad29yMEiAMVrqmxg130_provenance
;
np:hasPublicationInfo
dgn-np:NP588216.RAqUE9bE6r1bSP-o-t3AKh5YKZMQNad29yMEiAMVrqmxg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP588216.RAqUE9bE6r1bSP-o-t3AKh5YKZMQNad29yMEiAMVrqmxg130_assertion
a
np:Assertion
.
dgn-np:NP588216.RAqUE9bE6r1bSP-o-t3AKh5YKZMQNad29yMEiAMVrqmxg130_provenance
a
np:Provenance
.
dgn-np:NP588216.RAqUE9bE6r1bSP-o-t3AKh5YKZMQNad29yMEiAMVrqmxg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP588216.RAqUE9bE6r1bSP-o-t3AKh5YKZMQNad29yMEiAMVrqmxg130_assertion
{
miriam-gene:4763
a
ncit:C16612
.
lld:C0027832
a
ncit:C7057
.
dgn-gda:DGNa7d36fa1a35f2741a46c5c917c3e8fbd
sio:SIO_000628
miriam-gene:4763
,
lld:C0027832
;
a
sio:SIO_001121
.
}
dgn-np:NP588216.RAqUE9bE6r1bSP-o-t3AKh5YKZMQNad29yMEiAMVrqmxg130_provenance
{
dgn-np:NP588216.RAqUE9bE6r1bSP-o-t3AKh5YKZMQNad29yMEiAMVrqmxg130_assertion
dcterms:description
"[Inactivating NF2 mutations occur in several sporadic tumor types and have been linked to the NF2 disease, whose hallmark is the development of bilateral Schwann cell tumors (schwannomas) of the eighth cranial nerve.]. 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:9395247
;
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:NP588216.RAqUE9bE6r1bSP-o-t3AKh5YKZMQNad29yMEiAMVrqmxg130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:31+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" .
}