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http://rdf.disgenet.org/nanopublications.trig#NP237111.RArusIx3hAsGqS85dF8vHLI4k0erjapjO7OpQ2SNzYXuo
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
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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#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
np:hasAssertion
dgn-np:NP237111.RArusIx3hAsGqS85dF8vHLI4k0erjapjO7OpQ2SNzYXuo130_assertion
;
np:hasProvenance
dgn-np:NP237111.RArusIx3hAsGqS85dF8vHLI4k0erjapjO7OpQ2SNzYXuo130_provenance
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np:hasPublicationInfo
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;
a
np:Nanopublication
.
dgn-np:NP237111.RArusIx3hAsGqS85dF8vHLI4k0erjapjO7OpQ2SNzYXuo130_assertion
a
np:Assertion
.
dgn-np:NP237111.RArusIx3hAsGqS85dF8vHLI4k0erjapjO7OpQ2SNzYXuo130_provenance
a
np:Provenance
.
dgn-np:NP237111.RArusIx3hAsGqS85dF8vHLI4k0erjapjO7OpQ2SNzYXuo130_publicationInfo
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np:PublicationInfo
.
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dgn-np:NP237111.RArusIx3hAsGqS85dF8vHLI4k0erjapjO7OpQ2SNzYXuo130_assertion
{
miriam-gene:5925
a
ncit:C16612
.
lld:C0027831
a
ncit:C7057
.
dgn-gda:DGNe33dc9734a21373ec8e73bc44cdee53b
sio:SIO_000628
miriam-gene:5925
,
lld:C0027831
;
a
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.
}
dgn-np:NP237111.RArusIx3hAsGqS85dF8vHLI4k0erjapjO7OpQ2SNzYXuo130_provenance
{
dgn-np:NP237111.RArusIx3hAsGqS85dF8vHLI4k0erjapjO7OpQ2SNzYXuo130_assertion
dcterms:description
"[We have analyzed the somatic mutations in 89 cutaneous neurofibromas derived from three unrelated NF1 patients with high tumor burden, by loss of heterozygosity (LOH) analysis of the NF1, TP53, RB1, and CDKN2A genes, by assessing microsatellite instability (MSI), by direct sequencing of the NF1, TP53, and several mismatch repair (MMR) genes and by multiplex ligation-dependent probe amplification of the NF1 and TP53 genes.]. 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:20358387
;
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:NP237111.RArusIx3hAsGqS85dF8vHLI4k0erjapjO7OpQ2SNzYXuo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:13+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
<
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> ;
pav:version
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dgn-void:disgenetrdf
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}