@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP260481.RAaRQa2kkXFRkzxZ4GgEqSUOQMWtp03MYCcSEgwgFvRPI
> .
@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:NP260481.RAaRQa2kkXFRkzxZ4GgEqSUOQMWtp03MYCcSEgwgFvRPI130_head
{
this:
np:hasAssertion
dgn-np:NP260481.RAaRQa2kkXFRkzxZ4GgEqSUOQMWtp03MYCcSEgwgFvRPI130_assertion
;
np:hasProvenance
dgn-np:NP260481.RAaRQa2kkXFRkzxZ4GgEqSUOQMWtp03MYCcSEgwgFvRPI130_provenance
;
np:hasPublicationInfo
dgn-np:NP260481.RAaRQa2kkXFRkzxZ4GgEqSUOQMWtp03MYCcSEgwgFvRPI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP260481.RAaRQa2kkXFRkzxZ4GgEqSUOQMWtp03MYCcSEgwgFvRPI130_assertion
a
np:Assertion
.
dgn-np:NP260481.RAaRQa2kkXFRkzxZ4GgEqSUOQMWtp03MYCcSEgwgFvRPI130_provenance
a
np:Provenance
.
dgn-np:NP260481.RAaRQa2kkXFRkzxZ4GgEqSUOQMWtp03MYCcSEgwgFvRPI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP260481.RAaRQa2kkXFRkzxZ4GgEqSUOQMWtp03MYCcSEgwgFvRPI130_assertion
{
miriam-gene:4771
a
ncit:C16612
.
lld:C0027809
a
ncit:C7057
.
dgn-gda:DGNc648af5c0ff71ae3f9fbd26a5047e262
sio:SIO_000628
miriam-gene:4771
,
lld:C0027809
;
a
sio:SIO_001121
.
}
dgn-np:NP260481.RAaRQa2kkXFRkzxZ4GgEqSUOQMWtp03MYCcSEgwgFvRPI130_provenance
{
dgn-np:NP260481.RAaRQa2kkXFRkzxZ4GgEqSUOQMWtp03MYCcSEgwgFvRPI130_assertion
dcterms:description
"[Finally, no major differences were observed among tumors of different size, histological type or NF2 status, which suggests that, at the mRNA level, all schwannomas, regardless of their molecular and clinical characteristics, may share common features that can be used in their treatment.]. 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:23354516
;
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:NP260481.RAaRQa2kkXFRkzxZ4GgEqSUOQMWtp03MYCcSEgwgFvRPI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:25+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" .
}