@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP186515.RAITfChY1lFQci_uajnKhaSwyQyRpHLP30zr7GbDSKagI
> .
@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:NP186515.RAITfChY1lFQci_uajnKhaSwyQyRpHLP30zr7GbDSKagI130_head
{
this:
np:hasAssertion
dgn-np:NP186515.RAITfChY1lFQci_uajnKhaSwyQyRpHLP30zr7GbDSKagI130_assertion
;
np:hasProvenance
dgn-np:NP186515.RAITfChY1lFQci_uajnKhaSwyQyRpHLP30zr7GbDSKagI130_provenance
;
np:hasPublicationInfo
dgn-np:NP186515.RAITfChY1lFQci_uajnKhaSwyQyRpHLP30zr7GbDSKagI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP186515.RAITfChY1lFQci_uajnKhaSwyQyRpHLP30zr7GbDSKagI130_assertion
a
np:Assertion
.
dgn-np:NP186515.RAITfChY1lFQci_uajnKhaSwyQyRpHLP30zr7GbDSKagI130_provenance
a
np:Provenance
.
dgn-np:NP186515.RAITfChY1lFQci_uajnKhaSwyQyRpHLP30zr7GbDSKagI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP186515.RAITfChY1lFQci_uajnKhaSwyQyRpHLP30zr7GbDSKagI130_assertion
{
miriam-gene:200575
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGN743f3f2e6133a51de7979c761e578bd9
sio:SIO_000628
miriam-gene:200575
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP186515.RAITfChY1lFQci_uajnKhaSwyQyRpHLP30zr7GbDSKagI130_provenance
{
dgn-np:NP186515.RAITfChY1lFQci_uajnKhaSwyQyRpHLP30zr7GbDSKagI130_assertion
dcterms:description
"[Columnar cell lesions (CCL) and atypical ductal hyperplasia (ADH) frequently coexist and share molecular changes with in situ and invasive components, suggesting that CCL and ADH may be precursors to breast 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:20107913
;
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:NP186515.RAITfChY1lFQci_uajnKhaSwyQyRpHLP30zr7GbDSKagI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:42+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" .
}