@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP692991.RARHiholloFDKNi7DtyjxT1zq-t_V7UUBcK3IlQd35_NY
> .
@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:NP692991.RARHiholloFDKNi7DtyjxT1zq-t_V7UUBcK3IlQd35_NY130_head
{
this:
np:hasAssertion
dgn-np:NP692991.RARHiholloFDKNi7DtyjxT1zq-t_V7UUBcK3IlQd35_NY130_assertion
;
np:hasProvenance
dgn-np:NP692991.RARHiholloFDKNi7DtyjxT1zq-t_V7UUBcK3IlQd35_NY130_provenance
;
np:hasPublicationInfo
dgn-np:NP692991.RARHiholloFDKNi7DtyjxT1zq-t_V7UUBcK3IlQd35_NY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP692991.RARHiholloFDKNi7DtyjxT1zq-t_V7UUBcK3IlQd35_NY130_assertion
a
np:Assertion
.
dgn-np:NP692991.RARHiholloFDKNi7DtyjxT1zq-t_V7UUBcK3IlQd35_NY130_provenance
a
np:Provenance
.
dgn-np:NP692991.RARHiholloFDKNi7DtyjxT1zq-t_V7UUBcK3IlQd35_NY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP692991.RARHiholloFDKNi7DtyjxT1zq-t_V7UUBcK3IlQd35_NY130_assertion
{
miriam-gene:4000
a
ncit:C16612
.
lld:C1134719
a
ncit:C7057
.
dgn-gda:DGN632ca6105e25ee27f52f5de303d6f7d9
sio:SIO_000628
miriam-gene:4000
,
lld:C1134719
;
a
sio:SIO_001121
.
}
dgn-np:NP692991.RARHiholloFDKNi7DtyjxT1zq-t_V7UUBcK3IlQd35_NY130_provenance
{
dgn-np:NP692991.RARHiholloFDKNi7DtyjxT1zq-t_V7UUBcK3IlQd35_NY130_assertion
dcterms:description
"[The aim of this study was to determine whether MGA is clonal and whether it harbours chromosomal aberrations similar to those found in matched invasive ductal carcinoma of no special type (IDC-NST).]. 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:19922592
;
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:NP692991.RARHiholloFDKNi7DtyjxT1zq-t_V7UUBcK3IlQd35_NY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:01+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" .
}