@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP684119.RA6ioDEOuIlf7Kbq1U3yd5_NNAUCuzgHvSybSBJd0Kfpo
> .
@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:NP684119.RA6ioDEOuIlf7Kbq1U3yd5_NNAUCuzgHvSybSBJd0Kfpo130_head
{
this:
np:hasAssertion
dgn-np:NP684119.RA6ioDEOuIlf7Kbq1U3yd5_NNAUCuzgHvSybSBJd0Kfpo130_assertion
;
np:hasProvenance
dgn-np:NP684119.RA6ioDEOuIlf7Kbq1U3yd5_NNAUCuzgHvSybSBJd0Kfpo130_provenance
;
np:hasPublicationInfo
dgn-np:NP684119.RA6ioDEOuIlf7Kbq1U3yd5_NNAUCuzgHvSybSBJd0Kfpo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP684119.RA6ioDEOuIlf7Kbq1U3yd5_NNAUCuzgHvSybSBJd0Kfpo130_assertion
a
np:Assertion
.
dgn-np:NP684119.RA6ioDEOuIlf7Kbq1U3yd5_NNAUCuzgHvSybSBJd0Kfpo130_provenance
a
np:Provenance
.
dgn-np:NP684119.RA6ioDEOuIlf7Kbq1U3yd5_NNAUCuzgHvSybSBJd0Kfpo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP684119.RA6ioDEOuIlf7Kbq1U3yd5_NNAUCuzgHvSybSBJd0Kfpo130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0027708
a
ncit:C7057
.
dgn-gda:DGN8f6e3383ae9e0ad98e40d3d063a38880
sio:SIO_000628
miriam-gene:3342
,
lld:C0027708
;
a
sio:SIO_001121
.
}
dgn-np:NP684119.RA6ioDEOuIlf7Kbq1U3yd5_NNAUCuzgHvSybSBJd0Kfpo130_provenance
{
dgn-np:NP684119.RA6ioDEOuIlf7Kbq1U3yd5_NNAUCuzgHvSybSBJd0Kfpo130_assertion
dcterms:description
"[Molecular cytogenetic techniques such as chromosomal comparative genomic hybridization (CGH) have improved the diagnosis of chromosomal aberrations in Wilms' tumor since they can provide results based on the analysis of DNA from nondividing 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:23412795
;
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:NP684119.RA6ioDEOuIlf7Kbq1U3yd5_NNAUCuzgHvSybSBJd0Kfpo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:56+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" .
}