@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP685556.RA9j38leQ6SNlFCcuVGavZQ0GIZmvzM6bYrdTDvYwU7YM
> .
@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:NP685556.RA9j38leQ6SNlFCcuVGavZQ0GIZmvzM6bYrdTDvYwU7YM130_head
{
this:
np:hasAssertion
dgn-np:NP685556.RA9j38leQ6SNlFCcuVGavZQ0GIZmvzM6bYrdTDvYwU7YM130_assertion
;
np:hasProvenance
dgn-np:NP685556.RA9j38leQ6SNlFCcuVGavZQ0GIZmvzM6bYrdTDvYwU7YM130_provenance
;
np:hasPublicationInfo
dgn-np:NP685556.RA9j38leQ6SNlFCcuVGavZQ0GIZmvzM6bYrdTDvYwU7YM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP685556.RA9j38leQ6SNlFCcuVGavZQ0GIZmvzM6bYrdTDvYwU7YM130_assertion
a
np:Assertion
.
dgn-np:NP685556.RA9j38leQ6SNlFCcuVGavZQ0GIZmvzM6bYrdTDvYwU7YM130_provenance
a
np:Provenance
.
dgn-np:NP685556.RA9j38leQ6SNlFCcuVGavZQ0GIZmvzM6bYrdTDvYwU7YM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP685556.RA9j38leQ6SNlFCcuVGavZQ0GIZmvzM6bYrdTDvYwU7YM130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0027831
a
ncit:C7057
.
dgn-gda:DGN631541e8654dca0b60733009c768227a
sio:SIO_000628
miriam-gene:1029
,
lld:C0027831
;
a
sio:SIO_001121
.
}
dgn-np:NP685556.RA9j38leQ6SNlFCcuVGavZQ0GIZmvzM6bYrdTDvYwU7YM130_provenance
{
dgn-np:NP685556.RA9j38leQ6SNlFCcuVGavZQ0GIZmvzM6bYrdTDvYwU7YM130_assertion
dcterms:description
"[We have explored this molecular heterogeneity by performing loss of heterozygosity (LOH) analysis of the NF1, TP53, RB1, PTEN, and CDKN2A genes on sections of 10 MPNSTs derived from 10 unrelated NF1 patients.]. 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:23244685
;
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:NP685556.RA9j38leQ6SNlFCcuVGavZQ0GIZmvzM6bYrdTDvYwU7YM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:57+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" .
}