@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP705343.RAOWIc0zt0Yftnh5opPvHpGbtw4eSY66tThltolL9FXNk
> .
@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:NP705343.RAOWIc0zt0Yftnh5opPvHpGbtw4eSY66tThltolL9FXNk130_head
{
this:
np:hasAssertion
dgn-np:NP705343.RAOWIc0zt0Yftnh5opPvHpGbtw4eSY66tThltolL9FXNk130_assertion
;
np:hasProvenance
dgn-np:NP705343.RAOWIc0zt0Yftnh5opPvHpGbtw4eSY66tThltolL9FXNk130_provenance
;
np:hasPublicationInfo
dgn-np:NP705343.RAOWIc0zt0Yftnh5opPvHpGbtw4eSY66tThltolL9FXNk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP705343.RAOWIc0zt0Yftnh5opPvHpGbtw4eSY66tThltolL9FXNk130_assertion
a
np:Assertion
.
dgn-np:NP705343.RAOWIc0zt0Yftnh5opPvHpGbtw4eSY66tThltolL9FXNk130_provenance
a
np:Provenance
.
dgn-np:NP705343.RAOWIc0zt0Yftnh5opPvHpGbtw4eSY66tThltolL9FXNk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP705343.RAOWIc0zt0Yftnh5opPvHpGbtw4eSY66tThltolL9FXNk130_assertion
{
miriam-gene:57026
a
ncit:C16612
.
lld:C0007124
a
ncit:C7057
.
dgn-gda:DGN157ae722cb12bf1cdf2fb9f72e57932b
sio:SIO_000628
miriam-gene:57026
,
lld:C0007124
;
a
sio:SIO_001121
.
}
dgn-np:NP705343.RAOWIc0zt0Yftnh5opPvHpGbtw4eSY66tThltolL9FXNk130_provenance
{
dgn-np:NP705343.RAOWIc0zt0Yftnh5opPvHpGbtw4eSY66tThltolL9FXNk130_assertion
dcterms:description
"[However, CIN might also cause genetic heterogeneity, which was revealed by the findings that LOH at some markers was observed only in the component of ductal carcinoma in situ but not in the invasive component of the same tumors.]. 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:10919664
;
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:NP705343.RAOWIc0zt0Yftnh5opPvHpGbtw4eSY66tThltolL9FXNk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:08+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" .
}