@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP450125.RA9DLWgQwxqtWCK-3p59vxPfNwmEWXXuzrKzWXxoBJYnw
> .
@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:NP450125.RA9DLWgQwxqtWCK-3p59vxPfNwmEWXXuzrKzWXxoBJYnw130_head
{
this:
np:hasAssertion
dgn-np:NP450125.RA9DLWgQwxqtWCK-3p59vxPfNwmEWXXuzrKzWXxoBJYnw130_assertion
;
np:hasProvenance
dgn-np:NP450125.RA9DLWgQwxqtWCK-3p59vxPfNwmEWXXuzrKzWXxoBJYnw130_provenance
;
np:hasPublicationInfo
dgn-np:NP450125.RA9DLWgQwxqtWCK-3p59vxPfNwmEWXXuzrKzWXxoBJYnw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP450125.RA9DLWgQwxqtWCK-3p59vxPfNwmEWXXuzrKzWXxoBJYnw130_assertion
a
np:Assertion
.
dgn-np:NP450125.RA9DLWgQwxqtWCK-3p59vxPfNwmEWXXuzrKzWXxoBJYnw130_provenance
a
np:Provenance
.
dgn-np:NP450125.RA9DLWgQwxqtWCK-3p59vxPfNwmEWXXuzrKzWXxoBJYnw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP450125.RA9DLWgQwxqtWCK-3p59vxPfNwmEWXXuzrKzWXxoBJYnw130_assertion
{
miriam-gene:84034
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGN09891a24d65143159843d3bdeb065488
sio:SIO_000628
miriam-gene:84034
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP450125.RA9DLWgQwxqtWCK-3p59vxPfNwmEWXXuzrKzWXxoBJYnw130_provenance
{
dgn-np:NP450125.RA9DLWgQwxqtWCK-3p59vxPfNwmEWXXuzrKzWXxoBJYnw130_assertion
dcterms:description
"[Lastly and most importantly methylation of EMILIN2 was associated with poorer clinical outcome in breast cancer and was strongly associated with estrogen receptor as well as progesterone receptor positive breast cancers.]. 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:20205715
;
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:NP450125.RA9DLWgQwxqtWCK-3p59vxPfNwmEWXXuzrKzWXxoBJYnw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:28+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" .
}