@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP708891.RAsSnd3ILp2mDnGr8yKg7tqaCofo4o3DiepKlXNcGIgX4
> .
@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:NP708891.RAsSnd3ILp2mDnGr8yKg7tqaCofo4o3DiepKlXNcGIgX4130_head
{
this:
np:hasAssertion
dgn-np:NP708891.RAsSnd3ILp2mDnGr8yKg7tqaCofo4o3DiepKlXNcGIgX4130_assertion
;
np:hasProvenance
dgn-np:NP708891.RAsSnd3ILp2mDnGr8yKg7tqaCofo4o3DiepKlXNcGIgX4130_provenance
;
np:hasPublicationInfo
dgn-np:NP708891.RAsSnd3ILp2mDnGr8yKg7tqaCofo4o3DiepKlXNcGIgX4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP708891.RAsSnd3ILp2mDnGr8yKg7tqaCofo4o3DiepKlXNcGIgX4130_assertion
a
np:Assertion
.
dgn-np:NP708891.RAsSnd3ILp2mDnGr8yKg7tqaCofo4o3DiepKlXNcGIgX4130_provenance
a
np:Provenance
.
dgn-np:NP708891.RAsSnd3ILp2mDnGr8yKg7tqaCofo4o3DiepKlXNcGIgX4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP708891.RAsSnd3ILp2mDnGr8yKg7tqaCofo4o3DiepKlXNcGIgX4130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0206754
a
ncit:C7057
.
dgn-gda:DGN27a0744ef3fa6efe5626bcf3689211c2
sio:SIO_000628
miriam-gene:3342
,
lld:C0206754
;
a
sio:SIO_001121
.
}
dgn-np:NP708891.RAsSnd3ILp2mDnGr8yKg7tqaCofo4o3DiepKlXNcGIgX4130_provenance
{
dgn-np:NP708891.RAsSnd3ILp2mDnGr8yKg7tqaCofo4o3DiepKlXNcGIgX4130_assertion
dcterms:description
"[We have studied copy number aberrations (CNAs) in 26 sporadic neuroendocrine tumours of the enteropancreatic system (12 foregut and 14 midgut tumours) by comparative genomic hybridisation (CGH), allowing simultaneous evaluation of the entire tumour genome.]. 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:11247899
;
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:NP708891.RAsSnd3ILp2mDnGr8yKg7tqaCofo4o3DiepKlXNcGIgX4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:10+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" .
}