@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1196076.RAtOJwLWi6V6WHn9ESE1rBjUX5c4EIUmSaBGyFqzPD58o
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1196076.RAtOJwLWi6V6WHn9ESE1rBjUX5c4EIUmSaBGyFqzPD58o130_head
{
this:
np:hasAssertion
dgn-np:NP1196076.RAtOJwLWi6V6WHn9ESE1rBjUX5c4EIUmSaBGyFqzPD58o130_assertion
;
np:hasProvenance
dgn-np:NP1196076.RAtOJwLWi6V6WHn9ESE1rBjUX5c4EIUmSaBGyFqzPD58o130_provenance
;
np:hasPublicationInfo
dgn-np:NP1196076.RAtOJwLWi6V6WHn9ESE1rBjUX5c4EIUmSaBGyFqzPD58o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1196076.RAtOJwLWi6V6WHn9ESE1rBjUX5c4EIUmSaBGyFqzPD58o130_assertion
a
np:Assertion
.
dgn-np:NP1196076.RAtOJwLWi6V6WHn9ESE1rBjUX5c4EIUmSaBGyFqzPD58o130_provenance
a
np:Provenance
.
dgn-np:NP1196076.RAtOJwLWi6V6WHn9ESE1rBjUX5c4EIUmSaBGyFqzPD58o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1196076.RAtOJwLWi6V6WHn9ESE1rBjUX5c4EIUmSaBGyFqzPD58o130_assertion
{
miriam-gene:2064
a
ncit:C16612
.
lld:C0153381
a
ncit:C7057
.
dgn-gda:DGNfa2dc8dbe824b0005f70612c249ca448
sio:SIO_000628
miriam-gene:2064
,
lld:C0153381
;
a
sio:SIO_001121
.
}
dgn-np:NP1196076.RAtOJwLWi6V6WHn9ESE1rBjUX5c4EIUmSaBGyFqzPD58o130_provenance
{
dgn-np:NP1196076.RAtOJwLWi6V6WHn9ESE1rBjUX5c4EIUmSaBGyFqzPD58o130_assertion
dcterms:description
"[Out of the 349 genes, 34 (including several S100 gene family members) were found to be deleted and 30 (containing NOTCH4, TP53 and ERBB2) were found as amplified in OSF and OC cases.]. 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:24969693
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1196076.RAtOJwLWi6V6WHn9ESE1rBjUX5c4EIUmSaBGyFqzPD58o130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:48+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}