@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP876857.RAyOQCXiV0WPIHii1sYWnhAyE3EcGZOZ-jBweMLoqU2f8
> .
@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:NP876857.RAyOQCXiV0WPIHii1sYWnhAyE3EcGZOZ-jBweMLoqU2f8130_head
{
this:
np:hasAssertion
dgn-np:NP876857.RAyOQCXiV0WPIHii1sYWnhAyE3EcGZOZ-jBweMLoqU2f8130_assertion
;
np:hasProvenance
dgn-np:NP876857.RAyOQCXiV0WPIHii1sYWnhAyE3EcGZOZ-jBweMLoqU2f8130_provenance
;
np:hasPublicationInfo
dgn-np:NP876857.RAyOQCXiV0WPIHii1sYWnhAyE3EcGZOZ-jBweMLoqU2f8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP876857.RAyOQCXiV0WPIHii1sYWnhAyE3EcGZOZ-jBweMLoqU2f8130_assertion
a
np:Assertion
.
dgn-np:NP876857.RAyOQCXiV0WPIHii1sYWnhAyE3EcGZOZ-jBweMLoqU2f8130_provenance
a
np:Provenance
.
dgn-np:NP876857.RAyOQCXiV0WPIHii1sYWnhAyE3EcGZOZ-jBweMLoqU2f8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP876857.RAyOQCXiV0WPIHii1sYWnhAyE3EcGZOZ-jBweMLoqU2f8130_assertion
{
miriam-gene:2064
a
ncit:C16612
.
lld:C0677898
a
ncit:C7057
.
dgn-gda:DGNb296d23231e9a4d1ebb5127d656e4a1b
sio:SIO_000628
miriam-gene:2064
,
lld:C0677898
;
a
sio:SIO_001121
.
}
dgn-np:NP876857.RAyOQCXiV0WPIHii1sYWnhAyE3EcGZOZ-jBweMLoqU2f8130_provenance
{
dgn-np:NP876857.RAyOQCXiV0WPIHii1sYWnhAyE3EcGZOZ-jBweMLoqU2f8130_assertion
dcterms:description
"[With the exception of the 17q21 (ERBB2) amplicon, the overall frequency of copy number alterations was higher in invasive tumors than that in DCIS, with several of them present only in invasive cancer.]. 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:16618726
;
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:NP876857.RAyOQCXiV0WPIHii1sYWnhAyE3EcGZOZ-jBweMLoqU2f8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:56+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" .
}