@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP240656.RArYOBDbDCZ03WvABxPqoInmlDEoe7vO5Pd0_K6n6vdvM
> .
@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:NP240656.RArYOBDbDCZ03WvABxPqoInmlDEoe7vO5Pd0_K6n6vdvM130_head
{
this:
np:hasAssertion
dgn-np:NP240656.RArYOBDbDCZ03WvABxPqoInmlDEoe7vO5Pd0_K6n6vdvM130_assertion
;
np:hasProvenance
dgn-np:NP240656.RArYOBDbDCZ03WvABxPqoInmlDEoe7vO5Pd0_K6n6vdvM130_provenance
;
np:hasPublicationInfo
dgn-np:NP240656.RArYOBDbDCZ03WvABxPqoInmlDEoe7vO5Pd0_K6n6vdvM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP240656.RArYOBDbDCZ03WvABxPqoInmlDEoe7vO5Pd0_K6n6vdvM130_assertion
a
np:Assertion
.
dgn-np:NP240656.RArYOBDbDCZ03WvABxPqoInmlDEoe7vO5Pd0_K6n6vdvM130_provenance
a
np:Provenance
.
dgn-np:NP240656.RArYOBDbDCZ03WvABxPqoInmlDEoe7vO5Pd0_K6n6vdvM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP240656.RArYOBDbDCZ03WvABxPqoInmlDEoe7vO5Pd0_K6n6vdvM130_assertion
{
miriam-gene:7959
a
ncit:C16612
.
lld:C0007124
a
ncit:C7057
.
dgn-gda:DGN598ef9e6a40e3c529bec5e273d1e7587
sio:SIO_000628
miriam-gene:7959
,
lld:C0007124
;
a
sio:SIO_001121
.
}
dgn-np:NP240656.RArYOBDbDCZ03WvABxPqoInmlDEoe7vO5Pd0_K6n6vdvM130_provenance
{
dgn-np:NP240656.RArYOBDbDCZ03WvABxPqoInmlDEoe7vO5Pd0_K6n6vdvM130_assertion
dcterms:description
"[Four groups samples, including 40 cases of usual ductal hyperplasia (UDH), 40 cases of atypical ductal hyperplasia (ADH), 29 cases of flat epithelia atypia (FEA), and 40 cases of ductal carcinoma in situ (DCIS) were selected for analysis.]. 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:18425676
;
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:NP240656.RArYOBDbDCZ03WvABxPqoInmlDEoe7vO5Pd0_K6n6vdvM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:14+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" .
}