@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP908732.RAefWDIQlFPv3-UDEsc762X8S5Z5cQxoq5i2_VdTgRw9o
> .
@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:NP908732.RAefWDIQlFPv3-UDEsc762X8S5Z5cQxoq5i2_VdTgRw9o130_head
{
this:
np:hasAssertion
dgn-np:NP908732.RAefWDIQlFPv3-UDEsc762X8S5Z5cQxoq5i2_VdTgRw9o130_assertion
;
np:hasProvenance
dgn-np:NP908732.RAefWDIQlFPv3-UDEsc762X8S5Z5cQxoq5i2_VdTgRw9o130_provenance
;
np:hasPublicationInfo
dgn-np:NP908732.RAefWDIQlFPv3-UDEsc762X8S5Z5cQxoq5i2_VdTgRw9o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP908732.RAefWDIQlFPv3-UDEsc762X8S5Z5cQxoq5i2_VdTgRw9o130_assertion
a
np:Assertion
.
dgn-np:NP908732.RAefWDIQlFPv3-UDEsc762X8S5Z5cQxoq5i2_VdTgRw9o130_provenance
a
np:Provenance
.
dgn-np:NP908732.RAefWDIQlFPv3-UDEsc762X8S5Z5cQxoq5i2_VdTgRw9o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP908732.RAefWDIQlFPv3-UDEsc762X8S5Z5cQxoq5i2_VdTgRw9o130_assertion
{
miriam-gene:56946
a
ncit:C16612
.
lld:C1510420
a
ncit:C7057
.
dgn-gda:DGN33fa0ae3737f1fbe9661aacd93299177
sio:SIO_000628
miriam-gene:56946
,
lld:C1510420
;
a
sio:SIO_001121
.
}
dgn-np:NP908732.RAefWDIQlFPv3-UDEsc762X8S5Z5cQxoq5i2_VdTgRw9o130_provenance
{
dgn-np:NP908732.RAefWDIQlFPv3-UDEsc762X8S5Z5cQxoq5i2_VdTgRw9o130_assertion
dcterms:description
"[Microarray-based comparative genomic hybridization of cell lines from distinct tumour sites, including breast, ovary, pancreas, oesophagus, lung and the oral cavity, led to the identification of 10 cell lines with EMSY amplification and 18 without.]. 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:21735447
;
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:NP908732.RAefWDIQlFPv3-UDEsc762X8S5Z5cQxoq5i2_VdTgRw9o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:18+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" .
}