@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP729669.RAeOBRI2CNCQWjHfeqbf7mUcI3mgLDSdjsUZZpRejTQcI
> .
@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:NP729669.RAeOBRI2CNCQWjHfeqbf7mUcI3mgLDSdjsUZZpRejTQcI130_head
{
this:
np:hasAssertion
dgn-np:NP729669.RAeOBRI2CNCQWjHfeqbf7mUcI3mgLDSdjsUZZpRejTQcI130_assertion
;
np:hasProvenance
dgn-np:NP729669.RAeOBRI2CNCQWjHfeqbf7mUcI3mgLDSdjsUZZpRejTQcI130_provenance
;
np:hasPublicationInfo
dgn-np:NP729669.RAeOBRI2CNCQWjHfeqbf7mUcI3mgLDSdjsUZZpRejTQcI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP729669.RAeOBRI2CNCQWjHfeqbf7mUcI3mgLDSdjsUZZpRejTQcI130_assertion
a
np:Assertion
.
dgn-np:NP729669.RAeOBRI2CNCQWjHfeqbf7mUcI3mgLDSdjsUZZpRejTQcI130_provenance
a
np:Provenance
.
dgn-np:NP729669.RAeOBRI2CNCQWjHfeqbf7mUcI3mgLDSdjsUZZpRejTQcI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP729669.RAeOBRI2CNCQWjHfeqbf7mUcI3mgLDSdjsUZZpRejTQcI130_assertion
{
miriam-gene:57862
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGN541379f31a2d1d4f016695540ef65be5
sio:SIO_000628
miriam-gene:57862
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP729669.RAeOBRI2CNCQWjHfeqbf7mUcI3mgLDSdjsUZZpRejTQcI130_provenance
{
dgn-np:NP729669.RAeOBRI2CNCQWjHfeqbf7mUcI3mgLDSdjsUZZpRejTQcI130_assertion
dcterms:description
"[The high frequency of the VDR Apa1 A2/A2 homozygous polymorphism in women designated as elevated risk for breast cancer by the polyfactorial risk model might be related to the high incidence rates of breast cancer in Marin County, CA.]. 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:22867716
;
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:NP729669.RAeOBRI2CNCQWjHfeqbf7mUcI3mgLDSdjsUZZpRejTQcI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:23+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" .
}