@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP312266.RAvVwPijUFk-p2PjRWE3QKqOiAdPQDRLxYiTzoxjL30Ek
> .
@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/v4.0.0/void/
> .
dgn-np:NP312266.RAvVwPijUFk-p2PjRWE3QKqOiAdPQDRLxYiTzoxjL30Ek130_head
{
this:
np:hasAssertion
dgn-np:NP312266.RAvVwPijUFk-p2PjRWE3QKqOiAdPQDRLxYiTzoxjL30Ek130_assertion
;
np:hasProvenance
dgn-np:NP312266.RAvVwPijUFk-p2PjRWE3QKqOiAdPQDRLxYiTzoxjL30Ek130_provenance
;
np:hasPublicationInfo
dgn-np:NP312266.RAvVwPijUFk-p2PjRWE3QKqOiAdPQDRLxYiTzoxjL30Ek130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP312266.RAvVwPijUFk-p2PjRWE3QKqOiAdPQDRLxYiTzoxjL30Ek130_assertion
a
np:Assertion
.
dgn-np:NP312266.RAvVwPijUFk-p2PjRWE3QKqOiAdPQDRLxYiTzoxjL30Ek130_provenance
a
np:Provenance
.
dgn-np:NP312266.RAvVwPijUFk-p2PjRWE3QKqOiAdPQDRLxYiTzoxjL30Ek130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP312266.RAvVwPijUFk-p2PjRWE3QKqOiAdPQDRLxYiTzoxjL30Ek130_assertion
{
miriam-gene:4613
a
ncit:C16612
.
lld:C0027819
a
ncit:C7057
.
dgn-gda:DGN2a32fc39df1e705ecc9a38c6091b8e0a
sio:SIO_000628
miriam-gene:4613
,
lld:C0027819
;
a
sio:SIO_001121
.
}
dgn-np:NP312266.RAvVwPijUFk-p2PjRWE3QKqOiAdPQDRLxYiTzoxjL30Ek130_provenance
{
dgn-np:NP312266.RAvVwPijUFk-p2PjRWE3QKqOiAdPQDRLxYiTzoxjL30Ek130_assertion
dcterms:description
"[We performed loss of heterozygosity (LOH) analysis of 120 well characterized NB to better define specific regions of 1p loss and any association with clinical and biological prognostic features (DNA index, MYCN, age, and stage).]. 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:11272900
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP312266.RAvVwPijUFk-p2PjRWE3QKqOiAdPQDRLxYiTzoxjL30Ek130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:07+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}