@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP175222.RAlUS2cvaKruhsmBl4CirCN8a4K3GKofu5iOGH6O5g9VE
> .
@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:NP175222.RAlUS2cvaKruhsmBl4CirCN8a4K3GKofu5iOGH6O5g9VE130_head
{
this:
np:hasAssertion
dgn-np:NP175222.RAlUS2cvaKruhsmBl4CirCN8a4K3GKofu5iOGH6O5g9VE130_assertion
;
np:hasProvenance
dgn-np:NP175222.RAlUS2cvaKruhsmBl4CirCN8a4K3GKofu5iOGH6O5g9VE130_provenance
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np:hasPublicationInfo
dgn-np:NP175222.RAlUS2cvaKruhsmBl4CirCN8a4K3GKofu5iOGH6O5g9VE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP175222.RAlUS2cvaKruhsmBl4CirCN8a4K3GKofu5iOGH6O5g9VE130_assertion
a
np:Assertion
.
dgn-np:NP175222.RAlUS2cvaKruhsmBl4CirCN8a4K3GKofu5iOGH6O5g9VE130_provenance
a
np:Provenance
.
dgn-np:NP175222.RAlUS2cvaKruhsmBl4CirCN8a4K3GKofu5iOGH6O5g9VE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP175222.RAlUS2cvaKruhsmBl4CirCN8a4K3GKofu5iOGH6O5g9VE130_assertion
{
miriam-gene:4771
a
ncit:C16612
.
lld:C0178874
a
ncit:C7057
.
dgn-gda:DGN2213ee5078f9815b22265e125aed745d
sio:SIO_000628
miriam-gene:4771
,
lld:C0178874
;
a
sio:SIO_001121
.
}
dgn-np:NP175222.RAlUS2cvaKruhsmBl4CirCN8a4K3GKofu5iOGH6O5g9VE130_provenance
{
dgn-np:NP175222.RAlUS2cvaKruhsmBl4CirCN8a4K3GKofu5iOGH6O5g9VE130_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:NP175222.RAlUS2cvaKruhsmBl4CirCN8a4K3GKofu5iOGH6O5g9VE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:34+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
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