@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP923277.RANW8LmVn3DsWWlujSze249tBbGmLFM1nAb3MtMOhxy0Q
> .
@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:NP923277.RANW8LmVn3DsWWlujSze249tBbGmLFM1nAb3MtMOhxy0Q130_head
{
this:
np:hasAssertion
dgn-np:NP923277.RANW8LmVn3DsWWlujSze249tBbGmLFM1nAb3MtMOhxy0Q130_assertion
;
np:hasProvenance
dgn-np:NP923277.RANW8LmVn3DsWWlujSze249tBbGmLFM1nAb3MtMOhxy0Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP923277.RANW8LmVn3DsWWlujSze249tBbGmLFM1nAb3MtMOhxy0Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP923277.RANW8LmVn3DsWWlujSze249tBbGmLFM1nAb3MtMOhxy0Q130_assertion
a
np:Assertion
.
dgn-np:NP923277.RANW8LmVn3DsWWlujSze249tBbGmLFM1nAb3MtMOhxy0Q130_provenance
a
np:Provenance
.
dgn-np:NP923277.RANW8LmVn3DsWWlujSze249tBbGmLFM1nAb3MtMOhxy0Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP923277.RANW8LmVn3DsWWlujSze249tBbGmLFM1nAb3MtMOhxy0Q130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0302592
a
ncit:C7057
.
dgn-gda:DGN372f08f74819745539d1cf4e277b3864
sio:SIO_000628
miriam-gene:3342
,
lld:C0302592
;
a
sio:SIO_001121
.
}
dgn-np:NP923277.RANW8LmVn3DsWWlujSze249tBbGmLFM1nAb3MtMOhxy0Q130_provenance
{
dgn-np:NP923277.RANW8LmVn3DsWWlujSze249tBbGmLFM1nAb3MtMOhxy0Q130_assertion
dcterms:description
"[To identify chromosomal regions that may include the loci of abnormally expressed cellular genes and may be specifically altered depending on the histological subtype of the tumor, we studied primary cervical carcinoma using CGH and HPV genotyping.]. 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:10719846
;
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:NP923277.RANW8LmVn3DsWWlujSze249tBbGmLFM1nAb3MtMOhxy0Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:26+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" .
}