@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1334221.RAqbkntHrI47A8Vmxkjyj5wCFbbbLLpG3bm5zt4kvoWZ0
> .
@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:NP1334221.RAqbkntHrI47A8Vmxkjyj5wCFbbbLLpG3bm5zt4kvoWZ0130_head
{
this:
np:hasAssertion
dgn-np:NP1334221.RAqbkntHrI47A8Vmxkjyj5wCFbbbLLpG3bm5zt4kvoWZ0130_assertion
;
np:hasProvenance
dgn-np:NP1334221.RAqbkntHrI47A8Vmxkjyj5wCFbbbLLpG3bm5zt4kvoWZ0130_provenance
;
np:hasPublicationInfo
dgn-np:NP1334221.RAqbkntHrI47A8Vmxkjyj5wCFbbbLLpG3bm5zt4kvoWZ0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1334221.RAqbkntHrI47A8Vmxkjyj5wCFbbbLLpG3bm5zt4kvoWZ0130_assertion
a
np:Assertion
.
dgn-np:NP1334221.RAqbkntHrI47A8Vmxkjyj5wCFbbbLLpG3bm5zt4kvoWZ0130_provenance
a
np:Provenance
.
dgn-np:NP1334221.RAqbkntHrI47A8Vmxkjyj5wCFbbbLLpG3bm5zt4kvoWZ0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1334221.RAqbkntHrI47A8Vmxkjyj5wCFbbbLLpG3bm5zt4kvoWZ0130_assertion
{
miriam-gene:4771
a
ncit:C16612
.
lld:C0027859
a
ncit:C7057
.
dgn-gda:DGNa17fd3fd48a3001a30577ceb0077a8fb
sio:SIO_000628
miriam-gene:4771
,
lld:C0027859
;
a
sio:SIO_001121
.
}
dgn-np:NP1334221.RAqbkntHrI47A8Vmxkjyj5wCFbbbLLpG3bm5zt4kvoWZ0130_provenance
{
dgn-np:NP1334221.RAqbkntHrI47A8Vmxkjyj5wCFbbbLLpG3bm5zt4kvoWZ0130_assertion
dcterms:description
"[In this study we examined 61 schwannomas including 48 sporadic schwannomas (46 of which are vestibular schwannomas) and 12 schwannomas obtained from NF2 patients, for mutations in 10 of the 16 coding exons of the NF2 gene.]. 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:8162016
;
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:NP1334221.RAqbkntHrI47A8Vmxkjyj5wCFbbbLLpG3bm5zt4kvoWZ0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:51+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" .
}