@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP724120.RAgWSm7q9kqT86KmgWSXW95mduWLxX-inAEtk35MwNwt0
> .
@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:NP724120.RAgWSm7q9kqT86KmgWSXW95mduWLxX-inAEtk35MwNwt0130_head
{
this:
np:hasAssertion
dgn-np:NP724120.RAgWSm7q9kqT86KmgWSXW95mduWLxX-inAEtk35MwNwt0130_assertion
;
np:hasProvenance
dgn-np:NP724120.RAgWSm7q9kqT86KmgWSXW95mduWLxX-inAEtk35MwNwt0130_provenance
;
np:hasPublicationInfo
dgn-np:NP724120.RAgWSm7q9kqT86KmgWSXW95mduWLxX-inAEtk35MwNwt0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP724120.RAgWSm7q9kqT86KmgWSXW95mduWLxX-inAEtk35MwNwt0130_assertion
a
np:Assertion
.
dgn-np:NP724120.RAgWSm7q9kqT86KmgWSXW95mduWLxX-inAEtk35MwNwt0130_provenance
a
np:Provenance
.
dgn-np:NP724120.RAgWSm7q9kqT86KmgWSXW95mduWLxX-inAEtk35MwNwt0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP724120.RAgWSm7q9kqT86KmgWSXW95mduWLxX-inAEtk35MwNwt0130_assertion
{
miriam-gene:4000
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNa5ed3467ae37b72519e1ff3f18536c0c
sio:SIO_000628
miriam-gene:4000
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP724120.RAgWSm7q9kqT86KmgWSXW95mduWLxX-inAEtk35MwNwt0130_provenance
{
dgn-np:NP724120.RAgWSm7q9kqT86KmgWSXW95mduWLxX-inAEtk35MwNwt0130_assertion
dcterms:description
"[We confirm that the cancer phenotype develops early (in early hyperplasia or ADH stage) and find from our analysis that each subtype progresses from ADH to DCIS to IDC along its own specific pathway, as if each was a distinct disease.]. 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:17914245
;
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:NP724120.RAgWSm7q9kqT86KmgWSXW95mduWLxX-inAEtk35MwNwt0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:19+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" .
}