@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP170692.RAA-uJaLYNWLAOZnKtqnrGP6KDdogbzQ5EmFjnG9O6VnI
> .
@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:NP170692.RAA-uJaLYNWLAOZnKtqnrGP6KDdogbzQ5EmFjnG9O6VnI130_head
{
this:
np:hasAssertion
dgn-np:NP170692.RAA-uJaLYNWLAOZnKtqnrGP6KDdogbzQ5EmFjnG9O6VnI130_assertion
;
np:hasProvenance
dgn-np:NP170692.RAA-uJaLYNWLAOZnKtqnrGP6KDdogbzQ5EmFjnG9O6VnI130_provenance
;
np:hasPublicationInfo
dgn-np:NP170692.RAA-uJaLYNWLAOZnKtqnrGP6KDdogbzQ5EmFjnG9O6VnI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP170692.RAA-uJaLYNWLAOZnKtqnrGP6KDdogbzQ5EmFjnG9O6VnI130_assertion
a
np:Assertion
.
dgn-np:NP170692.RAA-uJaLYNWLAOZnKtqnrGP6KDdogbzQ5EmFjnG9O6VnI130_provenance
a
np:Provenance
.
dgn-np:NP170692.RAA-uJaLYNWLAOZnKtqnrGP6KDdogbzQ5EmFjnG9O6VnI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP170692.RAA-uJaLYNWLAOZnKtqnrGP6KDdogbzQ5EmFjnG9O6VnI130_assertion
{
miriam-gene:5241
a
ncit:C16612
.
lld:C0686619
a
ncit:C7057
.
dgn-gda:DGNa8ab38e0d5b52a81dc1f0bfbbb5e4ce3
sio:SIO_000628
miriam-gene:5241
,
lld:C0686619
;
a
sio:SIO_001121
.
}
dgn-np:NP170692.RAA-uJaLYNWLAOZnKtqnrGP6KDdogbzQ5EmFjnG9O6VnI130_provenance
{
dgn-np:NP170692.RAA-uJaLYNWLAOZnKtqnrGP6KDdogbzQ5EmFjnG9O6VnI130_assertion
dcterms:description
"[Association of the loss of heterozygosity/allelic imbalance, in both the stroma and epithelium, with presenting clinicopathological features, such as tumor grade, expression status of estrogen receptor and progesterone receptor, human epidermal growth factor receptor 2, clinical stage, and regional lymph node metastasis status.]. 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:17507346
;
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:NP170692.RAA-uJaLYNWLAOZnKtqnrGP6KDdogbzQ5EmFjnG9O6VnI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:32+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" .
}