@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP627544.RAbGFEUJ3P0za8ZixcgHJKBy9lu11o2hA0DzvtXSUwoHQ
> .
@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:NP627544.RAbGFEUJ3P0za8ZixcgHJKBy9lu11o2hA0DzvtXSUwoHQ130_head
{
this:
np:hasAssertion
dgn-np:NP627544.RAbGFEUJ3P0za8ZixcgHJKBy9lu11o2hA0DzvtXSUwoHQ130_assertion
;
np:hasProvenance
dgn-np:NP627544.RAbGFEUJ3P0za8ZixcgHJKBy9lu11o2hA0DzvtXSUwoHQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP627544.RAbGFEUJ3P0za8ZixcgHJKBy9lu11o2hA0DzvtXSUwoHQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP627544.RAbGFEUJ3P0za8ZixcgHJKBy9lu11o2hA0DzvtXSUwoHQ130_assertion
a
np:Assertion
.
dgn-np:NP627544.RAbGFEUJ3P0za8ZixcgHJKBy9lu11o2hA0DzvtXSUwoHQ130_provenance
a
np:Provenance
.
dgn-np:NP627544.RAbGFEUJ3P0za8ZixcgHJKBy9lu11o2hA0DzvtXSUwoHQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP627544.RAbGFEUJ3P0za8ZixcgHJKBy9lu11o2hA0DzvtXSUwoHQ130_assertion
{
miriam-gene:23512
a
ncit:C16612
.
lld:C0027831
a
ncit:C7057
.
dgn-gda:DGNbe8344c45b2330733f2157776d468eeb
sio:SIO_000628
miriam-gene:23512
,
lld:C0027831
;
a
sio:SIO_001121
.
}
dgn-np:NP627544.RAbGFEUJ3P0za8ZixcgHJKBy9lu11o2hA0DzvtXSUwoHQ130_provenance
{
dgn-np:NP627544.RAbGFEUJ3P0za8ZixcgHJKBy9lu11o2hA0DzvtXSUwoHQ130_assertion
dcterms:description
"[Although somatic inactivation of the NF1 wild-type allele is considered to be the PNF-initiating event in NF1 patients with intragenic mutations and patients with NF1 microdeletions, both patient groups may differ with regard to tumour progression because of the heterozygous constitutional deletion of SUZ12 present only in patients with NF1 microdeletions.]. 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:23101500
;
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:NP627544.RAbGFEUJ3P0za8ZixcgHJKBy9lu11o2hA0DzvtXSUwoHQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:18+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" .
}