@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP542440.RAHj2j5yvD6t7IrShvsUA_240PN8YASj2942GcEQ2AdKI
> .
@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:NP542440.RAHj2j5yvD6t7IrShvsUA_240PN8YASj2942GcEQ2AdKI130_head
{
this:
np:hasAssertion
dgn-np:NP542440.RAHj2j5yvD6t7IrShvsUA_240PN8YASj2942GcEQ2AdKI130_assertion
;
np:hasProvenance
dgn-np:NP542440.RAHj2j5yvD6t7IrShvsUA_240PN8YASj2942GcEQ2AdKI130_provenance
;
np:hasPublicationInfo
dgn-np:NP542440.RAHj2j5yvD6t7IrShvsUA_240PN8YASj2942GcEQ2AdKI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP542440.RAHj2j5yvD6t7IrShvsUA_240PN8YASj2942GcEQ2AdKI130_assertion
a
np:Assertion
.
dgn-np:NP542440.RAHj2j5yvD6t7IrShvsUA_240PN8YASj2942GcEQ2AdKI130_provenance
a
np:Provenance
.
dgn-np:NP542440.RAHj2j5yvD6t7IrShvsUA_240PN8YASj2942GcEQ2AdKI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP542440.RAHj2j5yvD6t7IrShvsUA_240PN8YASj2942GcEQ2AdKI130_assertion
{
miriam-gene:2099
a
ncit:C16612
.
lld:C1947901
a
ncit:C7057
.
dgn-gda:DGN84fa5f8e797352b97303dcfb03f97767
sio:SIO_000628
miriam-gene:2099
,
lld:C1947901
;
a
sio:SIO_001121
.
}
dgn-np:NP542440.RAHj2j5yvD6t7IrShvsUA_240PN8YASj2942GcEQ2AdKI130_provenance
{
dgn-np:NP542440.RAHj2j5yvD6t7IrShvsUA_240PN8YASj2942GcEQ2AdKI130_assertion
dcterms:description
"[Frequencies of SNPs were compared between cases and controls to identify SNPs associated with cancer susceptibility and between cases with different clinical phenotypes to determine the role of ESR1 polymorphism in cancer progression.]. 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:20570923
;
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:NP542440.RAHj2j5yvD6t7IrShvsUA_240PN8YASj2942GcEQ2AdKI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:27+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" .
}