@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP434734.RAKHdW4jcidSv182PFVa8WDclVKOk2MylfcF5DUG5BFms
> .
@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:NP434734.RAKHdW4jcidSv182PFVa8WDclVKOk2MylfcF5DUG5BFms130_head
{
this:
np:hasAssertion
dgn-np:NP434734.RAKHdW4jcidSv182PFVa8WDclVKOk2MylfcF5DUG5BFms130_assertion
;
np:hasProvenance
dgn-np:NP434734.RAKHdW4jcidSv182PFVa8WDclVKOk2MylfcF5DUG5BFms130_provenance
;
np:hasPublicationInfo
dgn-np:NP434734.RAKHdW4jcidSv182PFVa8WDclVKOk2MylfcF5DUG5BFms130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP434734.RAKHdW4jcidSv182PFVa8WDclVKOk2MylfcF5DUG5BFms130_assertion
a
np:Assertion
.
dgn-np:NP434734.RAKHdW4jcidSv182PFVa8WDclVKOk2MylfcF5DUG5BFms130_provenance
a
np:Provenance
.
dgn-np:NP434734.RAKHdW4jcidSv182PFVa8WDclVKOk2MylfcF5DUG5BFms130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP434734.RAKHdW4jcidSv182PFVa8WDclVKOk2MylfcF5DUG5BFms130_assertion
{
miriam-gene:672
a
ncit:C16612
.
lld:C1332347
a
ncit:C7057
.
dgn-gda:DGN0329aeaf42b7572dd6c7042e1a69c9af
sio:SIO_000628
miriam-gene:672
,
lld:C1332347
;
a
sio:SIO_001121
.
}
dgn-np:NP434734.RAKHdW4jcidSv182PFVa8WDclVKOk2MylfcF5DUG5BFms130_provenance
{
dgn-np:NP434734.RAKHdW4jcidSv182PFVa8WDclVKOk2MylfcF5DUG5BFms130_assertion
dcterms:description
"[In this review, progress in the understanding of lobular carcinoma in situ and atypical ductal hyperplasia, the use of the molecular marker CerbB2, and information gained from the morphological analysis of tumours arising in patients with BRCA1 and BRCA2 mutations is discussed.]. 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:11577167
;
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:NP434734.RAKHdW4jcidSv182PFVa8WDclVKOk2MylfcF5DUG5BFms130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:17+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" .
}