@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP187396.RAjpLu0JwP91nt_fwFBq6YXpwB3-8XwpJ4qAB0YtDmjpE
> .
@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:NP187396.RAjpLu0JwP91nt_fwFBq6YXpwB3-8XwpJ4qAB0YtDmjpE130_head
{
this:
np:hasAssertion
dgn-np:NP187396.RAjpLu0JwP91nt_fwFBq6YXpwB3-8XwpJ4qAB0YtDmjpE130_assertion
;
np:hasProvenance
dgn-np:NP187396.RAjpLu0JwP91nt_fwFBq6YXpwB3-8XwpJ4qAB0YtDmjpE130_provenance
;
np:hasPublicationInfo
dgn-np:NP187396.RAjpLu0JwP91nt_fwFBq6YXpwB3-8XwpJ4qAB0YtDmjpE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP187396.RAjpLu0JwP91nt_fwFBq6YXpwB3-8XwpJ4qAB0YtDmjpE130_assertion
a
np:Assertion
.
dgn-np:NP187396.RAjpLu0JwP91nt_fwFBq6YXpwB3-8XwpJ4qAB0YtDmjpE130_provenance
a
np:Provenance
.
dgn-np:NP187396.RAjpLu0JwP91nt_fwFBq6YXpwB3-8XwpJ4qAB0YtDmjpE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP187396.RAjpLu0JwP91nt_fwFBq6YXpwB3-8XwpJ4qAB0YtDmjpE130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN06c5b4e99cdfa4c0785d3773d5588397
sio:SIO_000628
miriam-gene:3342
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP187396.RAjpLu0JwP91nt_fwFBq6YXpwB3-8XwpJ4qAB0YtDmjpE130_provenance
{
dgn-np:NP187396.RAjpLu0JwP91nt_fwFBq6YXpwB3-8XwpJ4qAB0YtDmjpE130_assertion
dcterms:description
"[The molecular cytogenetic techniques of fluorescent in situ hybridization (FISH), comparative genomic hybridization (CGH), and spectral karyotyping (SKY) are providing tremendous insights into genetic information related to cancer by specifically illustrating chromosomal abnormalities that can occur in a patient's cancer cells.]. 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:11899766
;
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:NP187396.RAjpLu0JwP91nt_fwFBq6YXpwB3-8XwpJ4qAB0YtDmjpE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:43+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" .
}