@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP224756.RAWWFUmLQTM1Kwf7BHyFmH6TP0VjWgD4OAmATxRL_3Gg8
> .
@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:NP224756.RAWWFUmLQTM1Kwf7BHyFmH6TP0VjWgD4OAmATxRL_3Gg8130_head
{
this:
np:hasAssertion
dgn-np:NP224756.RAWWFUmLQTM1Kwf7BHyFmH6TP0VjWgD4OAmATxRL_3Gg8130_assertion
;
np:hasProvenance
dgn-np:NP224756.RAWWFUmLQTM1Kwf7BHyFmH6TP0VjWgD4OAmATxRL_3Gg8130_provenance
;
np:hasPublicationInfo
dgn-np:NP224756.RAWWFUmLQTM1Kwf7BHyFmH6TP0VjWgD4OAmATxRL_3Gg8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP224756.RAWWFUmLQTM1Kwf7BHyFmH6TP0VjWgD4OAmATxRL_3Gg8130_assertion
a
np:Assertion
.
dgn-np:NP224756.RAWWFUmLQTM1Kwf7BHyFmH6TP0VjWgD4OAmATxRL_3Gg8130_provenance
a
np:Provenance
.
dgn-np:NP224756.RAWWFUmLQTM1Kwf7BHyFmH6TP0VjWgD4OAmATxRL_3Gg8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP224756.RAWWFUmLQTM1Kwf7BHyFmH6TP0VjWgD4OAmATxRL_3Gg8130_assertion
{
miriam-gene:1594
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGN286a57abbaf4a3ac14ba34b2f89e9649
sio:SIO_000628
miriam-gene:1594
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP224756.RAWWFUmLQTM1Kwf7BHyFmH6TP0VjWgD4OAmATxRL_3Gg8130_provenance
{
dgn-np:NP224756.RAWWFUmLQTM1Kwf7BHyFmH6TP0VjWgD4OAmATxRL_3Gg8130_assertion
dcterms:description
"[Whatever the molecular mechanisms underlying the VDR effects in cancer cells, we believe that the VDR gene polymorphism may represent an important determinant in the evaluation of women affected by breast cancer and might help design targeted therapy.]. 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:9613456
;
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:NP224756.RAWWFUmLQTM1Kwf7BHyFmH6TP0VjWgD4OAmATxRL_3Gg8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:04+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" .
}