@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP305553.RAKjlLG1TMhj-Kv03M6hvavmgzdq9yI0RRDKkXD69FVgs
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
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{
this:
np:hasAssertion
dgn-np:NP305553.RAKjlLG1TMhj-Kv03M6hvavmgzdq9yI0RRDKkXD69FVgs130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP305553.RAKjlLG1TMhj-Kv03M6hvavmgzdq9yI0RRDKkXD69FVgs130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP305553.RAKjlLG1TMhj-Kv03M6hvavmgzdq9yI0RRDKkXD69FVgs130_assertion
a
np:Assertion
.
dgn-np:NP305553.RAKjlLG1TMhj-Kv03M6hvavmgzdq9yI0RRDKkXD69FVgs130_provenance
a
np:Provenance
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dgn-np:NP305553.RAKjlLG1TMhj-Kv03M6hvavmgzdq9yI0RRDKkXD69FVgs130_publicationInfo
a
np:PublicationInfo
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{
miriam-gene:1029
a
ncit:C16612
.
lld:C0206727
a
ncit:C7057
.
dgn-gda:DGN6f6c58434b93cdee8df0fa7809ebdad0
sio:SIO_000628
miriam-gene:1029
,
lld:C0206727
;
a
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.
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dgn-np:NP305553.RAKjlLG1TMhj-Kv03M6hvavmgzdq9yI0RRDKkXD69FVgs130_provenance
{
dgn-np:NP305553.RAKjlLG1TMhj-Kv03M6hvavmgzdq9yI0RRDKkXD69FVgs130_assertion
dcterms:description
"[Thus, we investigated the occurrence of TP53 and p16(INK4A) gene deregulation and the presence of microsatellite alterations at markers located at 17p, 17q, 9p21, 22q, 11q, 1p, or 2q loci in MPNSTs and neurofibromas either related (14 cases) or unrelated (14 cases) to NF1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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sio:SIO_000772
miriam-pubmed:11406645
;
prov:wasDerivedFrom
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;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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 .
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dgn-np:NP305553.RAKjlLG1TMhj-Kv03M6hvavmgzdq9yI0RRDKkXD69FVgs130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:40:35+02:00"^^
xsd:dateTime
;
dcterms:rights
<
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> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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pav:authoredBy
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
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pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
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