@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP571687.RAzR-EjS0kTm9mU22hjZehktxUMTH3BVGRteDLrqvdMUw
> .
@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:NP571687.RAzR-EjS0kTm9mU22hjZehktxUMTH3BVGRteDLrqvdMUw130_head
{
this:
np:hasAssertion
dgn-np:NP571687.RAzR-EjS0kTm9mU22hjZehktxUMTH3BVGRteDLrqvdMUw130_assertion
;
np:hasProvenance
dgn-np:NP571687.RAzR-EjS0kTm9mU22hjZehktxUMTH3BVGRteDLrqvdMUw130_provenance
;
np:hasPublicationInfo
dgn-np:NP571687.RAzR-EjS0kTm9mU22hjZehktxUMTH3BVGRteDLrqvdMUw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP571687.RAzR-EjS0kTm9mU22hjZehktxUMTH3BVGRteDLrqvdMUw130_assertion
a
np:Assertion
.
dgn-np:NP571687.RAzR-EjS0kTm9mU22hjZehktxUMTH3BVGRteDLrqvdMUw130_provenance
a
np:Provenance
.
dgn-np:NP571687.RAzR-EjS0kTm9mU22hjZehktxUMTH3BVGRteDLrqvdMUw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP571687.RAzR-EjS0kTm9mU22hjZehktxUMTH3BVGRteDLrqvdMUw130_assertion
{
miriam-gene:100653366
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN816c282a2d53fb098856062ab54de30f
sio:SIO_000628
miriam-gene:100653366
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP571687.RAzR-EjS0kTm9mU22hjZehktxUMTH3BVGRteDLrqvdMUw130_provenance
{
dgn-np:NP571687.RAzR-EjS0kTm9mU22hjZehktxUMTH3BVGRteDLrqvdMUw130_assertion
dcterms:description
"[Based on these observations, we propose that the presence of both PSC and aneuploidy in lymphocyte cultures of unaffected individuals from breast cancer families can be used as an important predictive parameter to determine the risk of developing 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:8972253
;
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:NP571687.RAzR-EjS0kTm9mU22hjZehktxUMTH3BVGRteDLrqvdMUw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:44+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" .
}