@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP807329.RAp7iT_daHAXMYjY6r5sLxF_oeJi-bIe1fXiGiDgLfeOI
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP807329.RAp7iT_daHAXMYjY6r5sLxF_oeJi-bIe1fXiGiDgLfeOI130_assertion
;
np:hasProvenance
dgn-np:NP807329.RAp7iT_daHAXMYjY6r5sLxF_oeJi-bIe1fXiGiDgLfeOI130_provenance
;
np:hasPublicationInfo
dgn-np:NP807329.RAp7iT_daHAXMYjY6r5sLxF_oeJi-bIe1fXiGiDgLfeOI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP807329.RAp7iT_daHAXMYjY6r5sLxF_oeJi-bIe1fXiGiDgLfeOI130_assertion
a
np:Assertion
.
dgn-np:NP807329.RAp7iT_daHAXMYjY6r5sLxF_oeJi-bIe1fXiGiDgLfeOI130_provenance
a
np:Provenance
.
dgn-np:NP807329.RAp7iT_daHAXMYjY6r5sLxF_oeJi-bIe1fXiGiDgLfeOI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP807329.RAp7iT_daHAXMYjY6r5sLxF_oeJi-bIe1fXiGiDgLfeOI130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0023473
a
ncit:C7057
.
dgn-gda:DGN341c295d1b47ce60a5fb2f3dff084774
sio:SIO_000628
miriam-gene:3342
,
lld:C0023473
;
a
sio:SIO_001121
.
}
dgn-np:NP807329.RAp7iT_daHAXMYjY6r5sLxF_oeJi-bIe1fXiGiDgLfeOI130_provenance
{
dgn-np:NP807329.RAp7iT_daHAXMYjY6r5sLxF_oeJi-bIe1fXiGiDgLfeOI130_assertion
dcterms:description
"[For validation of the array DNA samples of gastroesophageal and prostate cancer cell lines, and chronic myeloid leukemia specimens were used, which were previously characterized by multicolor fluorescence in situ hybridization and conventional CGH.]. 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:15619731
;
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:NP807329.RAp7iT_daHAXMYjY6r5sLxF_oeJi-bIe1fXiGiDgLfeOI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:15+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" .
}