@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP391013.RARBCmXZ-fCcWrfUnrvo-LgmEQJESvjplA21TnNVD3g6w
> .
@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:NP391013.RARBCmXZ-fCcWrfUnrvo-LgmEQJESvjplA21TnNVD3g6w130_head
{
this:
np:hasAssertion
dgn-np:NP391013.RARBCmXZ-fCcWrfUnrvo-LgmEQJESvjplA21TnNVD3g6w130_assertion
;
np:hasProvenance
dgn-np:NP391013.RARBCmXZ-fCcWrfUnrvo-LgmEQJESvjplA21TnNVD3g6w130_provenance
;
np:hasPublicationInfo
dgn-np:NP391013.RARBCmXZ-fCcWrfUnrvo-LgmEQJESvjplA21TnNVD3g6w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP391013.RARBCmXZ-fCcWrfUnrvo-LgmEQJESvjplA21TnNVD3g6w130_assertion
a
np:Assertion
.
dgn-np:NP391013.RARBCmXZ-fCcWrfUnrvo-LgmEQJESvjplA21TnNVD3g6w130_provenance
a
np:Provenance
.
dgn-np:NP391013.RARBCmXZ-fCcWrfUnrvo-LgmEQJESvjplA21TnNVD3g6w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP391013.RARBCmXZ-fCcWrfUnrvo-LgmEQJESvjplA21TnNVD3g6w130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0206727
a
ncit:C7057
.
dgn-gda:DGNadda0d439c06fc8a741049de0ee494e8
sio:SIO_000628
miriam-gene:3342
,
lld:C0206727
;
a
sio:SIO_001121
.
}
dgn-np:NP391013.RARBCmXZ-fCcWrfUnrvo-LgmEQJESvjplA21TnNVD3g6w130_provenance
{
dgn-np:NP391013.RARBCmXZ-fCcWrfUnrvo-LgmEQJESvjplA21TnNVD3g6w130_assertion
dcterms:description
"[Comparative genomic hybridization (CGH) was used to detect changes in relative chromosome copy number in 50 cases of peripheral nerve sheath tumour (PNSTs), including nine malignant peripheral nerve sheath tumours (MPNSTs), 27 neurofibromas (with three plexiform neurofibromas) and 14 schwannomas.]. 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:12081210
;
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:NP391013.RARBCmXZ-fCcWrfUnrvo-LgmEQJESvjplA21TnNVD3g6w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:53+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" .
}