@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP184428.RAAvdQwfj4BSRI_NC0V1Tvo0JDNSAcuFtZrqouvTuhlBk
> .
@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:NP184428.RAAvdQwfj4BSRI_NC0V1Tvo0JDNSAcuFtZrqouvTuhlBk130_head
{
this:
np:hasAssertion
dgn-np:NP184428.RAAvdQwfj4BSRI_NC0V1Tvo0JDNSAcuFtZrqouvTuhlBk130_assertion
;
np:hasProvenance
dgn-np:NP184428.RAAvdQwfj4BSRI_NC0V1Tvo0JDNSAcuFtZrqouvTuhlBk130_provenance
;
np:hasPublicationInfo
dgn-np:NP184428.RAAvdQwfj4BSRI_NC0V1Tvo0JDNSAcuFtZrqouvTuhlBk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP184428.RAAvdQwfj4BSRI_NC0V1Tvo0JDNSAcuFtZrqouvTuhlBk130_assertion
a
np:Assertion
.
dgn-np:NP184428.RAAvdQwfj4BSRI_NC0V1Tvo0JDNSAcuFtZrqouvTuhlBk130_provenance
a
np:Provenance
.
dgn-np:NP184428.RAAvdQwfj4BSRI_NC0V1Tvo0JDNSAcuFtZrqouvTuhlBk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP184428.RAAvdQwfj4BSRI_NC0V1Tvo0JDNSAcuFtZrqouvTuhlBk130_assertion
{
miriam-gene:8289
a
ncit:C16612
.
lld:C0476089
a
ncit:C7057
.
dgn-gda:DGN6d36b501e327e8d038237eba55ff0a85
sio:SIO_000628
miriam-gene:8289
,
lld:C0476089
;
a
sio:SIO_001121
.
}
dgn-np:NP184428.RAAvdQwfj4BSRI_NC0V1Tvo0JDNSAcuFtZrqouvTuhlBk130_provenance
{
dgn-np:NP184428.RAAvdQwfj4BSRI_NC0V1Tvo0JDNSAcuFtZrqouvTuhlBk130_assertion
dcterms:description
"[ESR1 amplification is independent of known clinicopathological factors related to poor prognosis and PTEN, p53, HER2, MLH1, and ARID1A protein expression, suggesting ESR1 amplification may be an early event in endometrial carcinoma development.]. 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:24023309
;
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:NP184428.RAAvdQwfj4BSRI_NC0V1Tvo0JDNSAcuFtZrqouvTuhlBk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:39+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" .
}