@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP691607.RACnjlkrXqEK-76-1sT69gQW_gYKUuK_nq0dSNGTzV6Z8
> .
@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:NP691607.RACnjlkrXqEK-76-1sT69gQW_gYKUuK_nq0dSNGTzV6Z8130_head
{
this:
np:hasAssertion
dgn-np:NP691607.RACnjlkrXqEK-76-1sT69gQW_gYKUuK_nq0dSNGTzV6Z8130_assertion
;
np:hasProvenance
dgn-np:NP691607.RACnjlkrXqEK-76-1sT69gQW_gYKUuK_nq0dSNGTzV6Z8130_provenance
;
np:hasPublicationInfo
dgn-np:NP691607.RACnjlkrXqEK-76-1sT69gQW_gYKUuK_nq0dSNGTzV6Z8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP691607.RACnjlkrXqEK-76-1sT69gQW_gYKUuK_nq0dSNGTzV6Z8130_assertion
a
np:Assertion
.
dgn-np:NP691607.RACnjlkrXqEK-76-1sT69gQW_gYKUuK_nq0dSNGTzV6Z8130_provenance
a
np:Provenance
.
dgn-np:NP691607.RACnjlkrXqEK-76-1sT69gQW_gYKUuK_nq0dSNGTzV6Z8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP691607.RACnjlkrXqEK-76-1sT69gQW_gYKUuK_nq0dSNGTzV6Z8130_assertion
{
miriam-gene:4771
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGN5f3bc64c8fc5bc6c3bd009f50600d2f3
sio:SIO_000628
miriam-gene:4771
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP691607.RACnjlkrXqEK-76-1sT69gQW_gYKUuK_nq0dSNGTzV6Z8130_provenance
{
dgn-np:NP691607.RACnjlkrXqEK-76-1sT69gQW_gYKUuK_nq0dSNGTzV6Z8130_assertion
dcterms:description
"[We analysed 23 sporadic schwannomas for mutations in the NF2 gene and for the allelic status at 1p, 14q and 22q, as alterations of these genomic regions appear to be related to tumour progression in meningiomas, another NF2-associated neoplasm.]. 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:9852312
;
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:NP691607.RACnjlkrXqEK-76-1sT69gQW_gYKUuK_nq0dSNGTzV6Z8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:00+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" .
}