@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP625967.RAf_qc8wx6eCxrB-KVokfvjsp1qYKPVc2fqbopPdvzAgI
> .
@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:NP625967.RAf_qc8wx6eCxrB-KVokfvjsp1qYKPVc2fqbopPdvzAgI130_head
{
this:
np:hasAssertion
dgn-np:NP625967.RAf_qc8wx6eCxrB-KVokfvjsp1qYKPVc2fqbopPdvzAgI130_assertion
;
np:hasProvenance
dgn-np:NP625967.RAf_qc8wx6eCxrB-KVokfvjsp1qYKPVc2fqbopPdvzAgI130_provenance
;
np:hasPublicationInfo
dgn-np:NP625967.RAf_qc8wx6eCxrB-KVokfvjsp1qYKPVc2fqbopPdvzAgI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP625967.RAf_qc8wx6eCxrB-KVokfvjsp1qYKPVc2fqbopPdvzAgI130_assertion
a
np:Assertion
.
dgn-np:NP625967.RAf_qc8wx6eCxrB-KVokfvjsp1qYKPVc2fqbopPdvzAgI130_provenance
a
np:Provenance
.
dgn-np:NP625967.RAf_qc8wx6eCxrB-KVokfvjsp1qYKPVc2fqbopPdvzAgI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP625967.RAf_qc8wx6eCxrB-KVokfvjsp1qYKPVc2fqbopPdvzAgI130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0027830
a
ncit:C7057
.
dgn-gda:DGN64ad54bae04ddd69a73d0fc605e67cb3
sio:SIO_000628
miriam-gene:7157
,
lld:C0027830
;
a
sio:SIO_001121
.
}
dgn-np:NP625967.RAf_qc8wx6eCxrB-KVokfvjsp1qYKPVc2fqbopPdvzAgI130_provenance
{
dgn-np:NP625967.RAf_qc8wx6eCxrB-KVokfvjsp1qYKPVc2fqbopPdvzAgI130_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 ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:11406645
;
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:NP625967.RAf_qc8wx6eCxrB-KVokfvjsp1qYKPVc2fqbopPdvzAgI130_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" .
}