@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP559998.RAbvyG-bIy0EkyN90eX0hAwbg7E8h0bkL-7py00xWxlWY
> .
@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:NP559998.RAbvyG-bIy0EkyN90eX0hAwbg7E8h0bkL-7py00xWxlWY130_head
{
this:
np:hasAssertion
dgn-np:NP559998.RAbvyG-bIy0EkyN90eX0hAwbg7E8h0bkL-7py00xWxlWY130_assertion
;
np:hasProvenance
dgn-np:NP559998.RAbvyG-bIy0EkyN90eX0hAwbg7E8h0bkL-7py00xWxlWY130_provenance
;
np:hasPublicationInfo
dgn-np:NP559998.RAbvyG-bIy0EkyN90eX0hAwbg7E8h0bkL-7py00xWxlWY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP559998.RAbvyG-bIy0EkyN90eX0hAwbg7E8h0bkL-7py00xWxlWY130_assertion
a
np:Assertion
.
dgn-np:NP559998.RAbvyG-bIy0EkyN90eX0hAwbg7E8h0bkL-7py00xWxlWY130_provenance
a
np:Provenance
.
dgn-np:NP559998.RAbvyG-bIy0EkyN90eX0hAwbg7E8h0bkL-7py00xWxlWY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP559998.RAbvyG-bIy0EkyN90eX0hAwbg7E8h0bkL-7py00xWxlWY130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C0750974
a
ncit:C7057
.
dgn-gda:DGN3255f7804b2440268a7e500cbb8797f7
sio:SIO_000628
miriam-gene:1956
,
lld:C0750974
;
a
sio:SIO_001121
.
}
dgn-np:NP559998.RAbvyG-bIy0EkyN90eX0hAwbg7E8h0bkL-7py00xWxlWY130_provenance
{
dgn-np:NP559998.RAbvyG-bIy0EkyN90eX0hAwbg7E8h0bkL-7py00xWxlWY130_assertion
dcterms:description
"[In order to evaluate the incidence and prognostic significance of gene amplification in primary brain neoplasms we measured the number of gene copies per cell of three oncogenes (epidermal growth factor receptor [EGFR] gene, N-myc, C-myc) and syntenic control genes in 40 specimens using quantitative DNA dot blots.]. 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:1311022
;
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:NP559998.RAbvyG-bIy0EkyN90eX0hAwbg7E8h0bkL-7py00xWxlWY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:37+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" .
}