@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP256137.RAUeCd7KQgLrW-QzHf78QCpN3FEZpxKtyTMUH2z8WS9V4
> .
@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:NP256137.RAUeCd7KQgLrW-QzHf78QCpN3FEZpxKtyTMUH2z8WS9V4130_head
{
this:
np:hasAssertion
dgn-np:NP256137.RAUeCd7KQgLrW-QzHf78QCpN3FEZpxKtyTMUH2z8WS9V4130_assertion
;
np:hasProvenance
dgn-np:NP256137.RAUeCd7KQgLrW-QzHf78QCpN3FEZpxKtyTMUH2z8WS9V4130_provenance
;
np:hasPublicationInfo
dgn-np:NP256137.RAUeCd7KQgLrW-QzHf78QCpN3FEZpxKtyTMUH2z8WS9V4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP256137.RAUeCd7KQgLrW-QzHf78QCpN3FEZpxKtyTMUH2z8WS9V4130_assertion
a
np:Assertion
.
dgn-np:NP256137.RAUeCd7KQgLrW-QzHf78QCpN3FEZpxKtyTMUH2z8WS9V4130_provenance
a
np:Provenance
.
dgn-np:NP256137.RAUeCd7KQgLrW-QzHf78QCpN3FEZpxKtyTMUH2z8WS9V4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP256137.RAUeCd7KQgLrW-QzHf78QCpN3FEZpxKtyTMUH2z8WS9V4130_assertion
{
miriam-gene:595
a
ncit:C16612
.
lld:C1961102
a
ncit:C7057
.
dgn-gda:DGNd9c30decf1152ee32188d55fb413ce7f
sio:SIO_000628
miriam-gene:595
,
lld:C1961102
;
a
sio:SIO_001121
.
}
dgn-np:NP256137.RAUeCd7KQgLrW-QzHf78QCpN3FEZpxKtyTMUH2z8WS9V4130_provenance
{
dgn-np:NP256137.RAUeCd7KQgLrW-QzHf78QCpN3FEZpxKtyTMUH2z8WS9V4130_assertion
dcterms:description
"[To study the association between cyclin D1 (CCND1) polymorphic variants and acute lymphoblastic leukemia (ALL) and breast cancer cases and the possibility of having different (CCND1) polymorphic variants in the development of ALL and breast 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: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:NP256137.RAUeCd7KQgLrW-QzHf78QCpN3FEZpxKtyTMUH2z8WS9V4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:23+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" .
}