@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP248399.RAZfH4R0VpVsg5oCNUlAIPsof5meLIuzvvJ5dFGyvjZ8E
> .
@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:NP248399.RAZfH4R0VpVsg5oCNUlAIPsof5meLIuzvvJ5dFGyvjZ8E130_head
{
this:
np:hasAssertion
dgn-np:NP248399.RAZfH4R0VpVsg5oCNUlAIPsof5meLIuzvvJ5dFGyvjZ8E130_assertion
;
np:hasProvenance
dgn-np:NP248399.RAZfH4R0VpVsg5oCNUlAIPsof5meLIuzvvJ5dFGyvjZ8E130_provenance
;
np:hasPublicationInfo
dgn-np:NP248399.RAZfH4R0VpVsg5oCNUlAIPsof5meLIuzvvJ5dFGyvjZ8E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP248399.RAZfH4R0VpVsg5oCNUlAIPsof5meLIuzvvJ5dFGyvjZ8E130_assertion
a
np:Assertion
.
dgn-np:NP248399.RAZfH4R0VpVsg5oCNUlAIPsof5meLIuzvvJ5dFGyvjZ8E130_provenance
a
np:Provenance
.
dgn-np:NP248399.RAZfH4R0VpVsg5oCNUlAIPsof5meLIuzvvJ5dFGyvjZ8E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP248399.RAZfH4R0VpVsg5oCNUlAIPsof5meLIuzvvJ5dFGyvjZ8E130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0010701
a
ncit:C7057
.
dgn-gda:DGN9c6e7548030a4cc3d24e9aba13a87055
sio:SIO_000628
miriam-gene:3342
,
lld:C0010701
;
a
sio:SIO_001121
.
}
dgn-np:NP248399.RAZfH4R0VpVsg5oCNUlAIPsof5meLIuzvvJ5dFGyvjZ8E130_provenance
{
dgn-np:NP248399.RAZfH4R0VpVsg5oCNUlAIPsof5meLIuzvvJ5dFGyvjZ8E130_assertion
dcterms:description
"[We studied DNA copy number changes by CGH and allelic imbalance (AI) on 3p by LOH analysis on 22 phyllodes tumours (PT) of the breast in order to gain insight into the genetic basis of tumour progression in PT.]. 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:12632018
;
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:NP248399.RAZfH4R0VpVsg5oCNUlAIPsof5meLIuzvvJ5dFGyvjZ8E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:19+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" .
}