@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP476365.RA-HRiRC6FMenOKVzi68geLe4nwRkySXyRIgA6yOlx2ww
> .
@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:NP476365.RA-HRiRC6FMenOKVzi68geLe4nwRkySXyRIgA6yOlx2ww130_head
{
this:
np:hasAssertion
dgn-np:NP476365.RA-HRiRC6FMenOKVzi68geLe4nwRkySXyRIgA6yOlx2ww130_assertion
;
np:hasProvenance
dgn-np:NP476365.RA-HRiRC6FMenOKVzi68geLe4nwRkySXyRIgA6yOlx2ww130_provenance
;
np:hasPublicationInfo
dgn-np:NP476365.RA-HRiRC6FMenOKVzi68geLe4nwRkySXyRIgA6yOlx2ww130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP476365.RA-HRiRC6FMenOKVzi68geLe4nwRkySXyRIgA6yOlx2ww130_assertion
a
np:Assertion
.
dgn-np:NP476365.RA-HRiRC6FMenOKVzi68geLe4nwRkySXyRIgA6yOlx2ww130_provenance
a
np:Provenance
.
dgn-np:NP476365.RA-HRiRC6FMenOKVzi68geLe4nwRkySXyRIgA6yOlx2ww130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP476365.RA-HRiRC6FMenOKVzi68geLe4nwRkySXyRIgA6yOlx2ww130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0030421
a
ncit:C7057
.
dgn-gda:DGN9446ab944ca75f1de1288634294dcbd3
sio:SIO_000628
miriam-gene:3342
,
lld:C0030421
;
a
sio:SIO_001121
.
}
dgn-np:NP476365.RA-HRiRC6FMenOKVzi68geLe4nwRkySXyRIgA6yOlx2ww130_provenance
{
dgn-np:NP476365.RA-HRiRC6FMenOKVzi68geLe4nwRkySXyRIgA6yOlx2ww130_assertion
dcterms:description
"[To define new candidate regions, we performed CGH analysis on 29 pheochromocytomas and on 24 paragangliomas mainly of head and neck origin (20 of 24), which allowed us to differentiate between the two tumor types.]. 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:15609347
;
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:NP476365.RA-HRiRC6FMenOKVzi68geLe4nwRkySXyRIgA6yOlx2ww130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:45+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" .
}