@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP927305.RAEgisAfKPm4Cc5KCNEANz33xVyWf-lvFpYcNyXXo8Wao
> .
@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:NP927305.RAEgisAfKPm4Cc5KCNEANz33xVyWf-lvFpYcNyXXo8Wao130_head
{
this:
np:hasAssertion
dgn-np:NP927305.RAEgisAfKPm4Cc5KCNEANz33xVyWf-lvFpYcNyXXo8Wao130_assertion
;
np:hasProvenance
dgn-np:NP927305.RAEgisAfKPm4Cc5KCNEANz33xVyWf-lvFpYcNyXXo8Wao130_provenance
;
np:hasPublicationInfo
dgn-np:NP927305.RAEgisAfKPm4Cc5KCNEANz33xVyWf-lvFpYcNyXXo8Wao130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP927305.RAEgisAfKPm4Cc5KCNEANz33xVyWf-lvFpYcNyXXo8Wao130_assertion
a
np:Assertion
.
dgn-np:NP927305.RAEgisAfKPm4Cc5KCNEANz33xVyWf-lvFpYcNyXXo8Wao130_provenance
a
np:Provenance
.
dgn-np:NP927305.RAEgisAfKPm4Cc5KCNEANz33xVyWf-lvFpYcNyXXo8Wao130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP927305.RAEgisAfKPm4Cc5KCNEANz33xVyWf-lvFpYcNyXXo8Wao130_assertion
{
miriam-gene:595
a
ncit:C16612
.
lld:C0235653
a
ncit:C7057
.
dgn-gda:DGN9c924603de6f7e230dd097e5e8ad462c
sio:SIO_000628
miriam-gene:595
,
lld:C0235653
;
a
sio:SIO_001121
.
}
dgn-np:NP927305.RAEgisAfKPm4Cc5KCNEANz33xVyWf-lvFpYcNyXXo8Wao130_provenance
{
dgn-np:NP927305.RAEgisAfKPm4Cc5KCNEANz33xVyWf-lvFpYcNyXXo8Wao130_assertion
dcterms:description
"[We evaluated the association of CCND1 G870A polymorphism with ALL risk in 25 ALL patients and 15 healthy controls and with breast cancer risk in 30 newly diagnosed breast cancer female patients and in 25 healthy controls.]. 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:23613410
;
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:NP927305.RAEgisAfKPm4Cc5KCNEANz33xVyWf-lvFpYcNyXXo8Wao130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:28+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" .
}