@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP709336.RAH_Capp2PcicJomZRIHhhkCj7giUR-ulTBIl3k33xf-0
> .
@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:NP709336.RAH_Capp2PcicJomZRIHhhkCj7giUR-ulTBIl3k33xf-0130_head
{
this:
np:hasAssertion
dgn-np:NP709336.RAH_Capp2PcicJomZRIHhhkCj7giUR-ulTBIl3k33xf-0130_assertion
;
np:hasProvenance
dgn-np:NP709336.RAH_Capp2PcicJomZRIHhhkCj7giUR-ulTBIl3k33xf-0130_provenance
;
np:hasPublicationInfo
dgn-np:NP709336.RAH_Capp2PcicJomZRIHhhkCj7giUR-ulTBIl3k33xf-0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP709336.RAH_Capp2PcicJomZRIHhhkCj7giUR-ulTBIl3k33xf-0130_assertion
a
np:Assertion
.
dgn-np:NP709336.RAH_Capp2PcicJomZRIHhhkCj7giUR-ulTBIl3k33xf-0130_provenance
a
np:Provenance
.
dgn-np:NP709336.RAH_Capp2PcicJomZRIHhhkCj7giUR-ulTBIl3k33xf-0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP709336.RAH_Capp2PcicJomZRIHhhkCj7giUR-ulTBIl3k33xf-0130_assertion
{
miriam-gene:5781
a
ncit:C16612
.
lld:C0598766
a
ncit:C7057
.
dgn-gda:DGN72246dd2eafb05f03f88da1b86a0e3f1
sio:SIO_000628
miriam-gene:5781
,
lld:C0598766
;
a
sio:SIO_001121
.
}
dgn-np:NP709336.RAH_Capp2PcicJomZRIHhhkCj7giUR-ulTBIl3k33xf-0130_provenance
{
dgn-np:NP709336.RAH_Capp2PcicJomZRIHhhkCj7giUR-ulTBIl3k33xf-0130_assertion
dcterms:description
"[Although, we cannot conclude whether there is an association between NS and neuroblastoma, this case suggests that duplication of germline PTPN11 mutations, potentially induced by chemotherapy, contributes to leukemogenesis in patients with NS.]. 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:16078230
;
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:NP709336.RAH_Capp2PcicJomZRIHhhkCj7giUR-ulTBIl3k33xf-0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:11+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" .
}