@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP319368.RAYkibM2A_JPB2pfi_Gcw6OfrbmFlcwD3NnXNBHjDxbQk
> .
@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:NP319368.RAYkibM2A_JPB2pfi_Gcw6OfrbmFlcwD3NnXNBHjDxbQk130_head
{
this:
np:hasAssertion
dgn-np:NP319368.RAYkibM2A_JPB2pfi_Gcw6OfrbmFlcwD3NnXNBHjDxbQk130_assertion
;
np:hasProvenance
dgn-np:NP319368.RAYkibM2A_JPB2pfi_Gcw6OfrbmFlcwD3NnXNBHjDxbQk130_provenance
;
np:hasPublicationInfo
dgn-np:NP319368.RAYkibM2A_JPB2pfi_Gcw6OfrbmFlcwD3NnXNBHjDxbQk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP319368.RAYkibM2A_JPB2pfi_Gcw6OfrbmFlcwD3NnXNBHjDxbQk130_assertion
a
np:Assertion
.
dgn-np:NP319368.RAYkibM2A_JPB2pfi_Gcw6OfrbmFlcwD3NnXNBHjDxbQk130_provenance
a
np:Provenance
.
dgn-np:NP319368.RAYkibM2A_JPB2pfi_Gcw6OfrbmFlcwD3NnXNBHjDxbQk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP319368.RAYkibM2A_JPB2pfi_Gcw6OfrbmFlcwD3NnXNBHjDxbQk130_assertion
{
miriam-gene:4771
a
ncit:C16612
.
lld:C0027859
a
ncit:C7057
.
dgn-gda:DGN6965c089e4c3cca631bb8633e2b4ace5
sio:SIO_000628
miriam-gene:4771
,
lld:C0027859
;
a
sio:SIO_001121
.
}
dgn-np:NP319368.RAYkibM2A_JPB2pfi_Gcw6OfrbmFlcwD3NnXNBHjDxbQk130_provenance
{
dgn-np:NP319368.RAYkibM2A_JPB2pfi_Gcw6OfrbmFlcwD3NnXNBHjDxbQk130_assertion
dcterms:description
"[Although mutational inactivation and allelic loss in the NF2 gene appear to be causal events in the majority of vestibular schwannomas, involvement of another potentially important mechanism, transcriptional inactivation, has not been investigated.]. 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:11380622
;
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:NP319368.RAYkibM2A_JPB2pfi_Gcw6OfrbmFlcwD3NnXNBHjDxbQk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:10+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" .
}