@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP461126.RAd82YtWFza0cu44bnxvxZOig62-LHBzqIXTkrrszqBNw
> .
@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:NP461126.RAd82YtWFza0cu44bnxvxZOig62-LHBzqIXTkrrszqBNw130_head
{
this:
np:hasAssertion
dgn-np:NP461126.RAd82YtWFza0cu44bnxvxZOig62-LHBzqIXTkrrszqBNw130_assertion
;
np:hasProvenance
dgn-np:NP461126.RAd82YtWFza0cu44bnxvxZOig62-LHBzqIXTkrrszqBNw130_provenance
;
np:hasPublicationInfo
dgn-np:NP461126.RAd82YtWFza0cu44bnxvxZOig62-LHBzqIXTkrrszqBNw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP461126.RAd82YtWFza0cu44bnxvxZOig62-LHBzqIXTkrrszqBNw130_assertion
a
np:Assertion
.
dgn-np:NP461126.RAd82YtWFza0cu44bnxvxZOig62-LHBzqIXTkrrszqBNw130_provenance
a
np:Provenance
.
dgn-np:NP461126.RAd82YtWFza0cu44bnxvxZOig62-LHBzqIXTkrrszqBNw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP461126.RAd82YtWFza0cu44bnxvxZOig62-LHBzqIXTkrrszqBNw130_assertion
{
miriam-gene:4000
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN78fded3102bff5b62758ed9fa27704c1
sio:SIO_000628
miriam-gene:4000
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP461126.RAd82YtWFza0cu44bnxvxZOig62-LHBzqIXTkrrszqBNw130_provenance
{
dgn-np:NP461126.RAd82YtWFza0cu44bnxvxZOig62-LHBzqIXTkrrszqBNw130_assertion
dcterms:description
"[Although there was only a slight agreement of DNA copy number alterations between the primary tumor and the blood samples, the blood cell copy number variation may have some clinical significance as compared to the primary tumor in IDC breast cancer patients.]. 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:20409316
;
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:NP461126.RAd82YtWFza0cu44bnxvxZOig62-LHBzqIXTkrrszqBNw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:34+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" .
}