@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP358724.RAiNWuE5CUFNfSjBEbA-mrOYOhtxffPmYwbbnKtvqlJ9s
> .
@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:NP358724.RAiNWuE5CUFNfSjBEbA-mrOYOhtxffPmYwbbnKtvqlJ9s130_head
{
this:
np:hasAssertion
dgn-np:NP358724.RAiNWuE5CUFNfSjBEbA-mrOYOhtxffPmYwbbnKtvqlJ9s130_assertion
;
np:hasProvenance
dgn-np:NP358724.RAiNWuE5CUFNfSjBEbA-mrOYOhtxffPmYwbbnKtvqlJ9s130_provenance
;
np:hasPublicationInfo
dgn-np:NP358724.RAiNWuE5CUFNfSjBEbA-mrOYOhtxffPmYwbbnKtvqlJ9s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP358724.RAiNWuE5CUFNfSjBEbA-mrOYOhtxffPmYwbbnKtvqlJ9s130_assertion
a
np:Assertion
.
dgn-np:NP358724.RAiNWuE5CUFNfSjBEbA-mrOYOhtxffPmYwbbnKtvqlJ9s130_provenance
a
np:Provenance
.
dgn-np:NP358724.RAiNWuE5CUFNfSjBEbA-mrOYOhtxffPmYwbbnKtvqlJ9s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP358724.RAiNWuE5CUFNfSjBEbA-mrOYOhtxffPmYwbbnKtvqlJ9s130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C0025286
a
ncit:C7057
.
dgn-gda:DGN79188dca409511a905e98fa6eb9a8198
sio:SIO_000628
miriam-gene:7248
,
lld:C0025286
;
a
sio:SIO_001121
.
}
dgn-np:NP358724.RAiNWuE5CUFNfSjBEbA-mrOYOhtxffPmYwbbnKtvqlJ9s130_provenance
{
dgn-np:NP358724.RAiNWuE5CUFNfSjBEbA-mrOYOhtxffPmYwbbnKtvqlJ9s130_assertion
dcterms:description
"[Mutation analyses have revealed that the NF2 tumour suppressor gene is frequently mutated not only in vestibular schwannomas and meningiomas from NF2 patients, but also in their sporadic counterparts, which represent approximately one third of all human brain tumours.]. 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:8718520
;
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:NP358724.RAiNWuE5CUFNfSjBEbA-mrOYOhtxffPmYwbbnKtvqlJ9s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:30+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" .
}