@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP411378.RAHVMiE3J7puyUd2B71Z9hlXHseyq4KQ4U2vu2LKJ0_gI
> .
@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:NP411378.RAHVMiE3J7puyUd2B71Z9hlXHseyq4KQ4U2vu2LKJ0_gI130_head
{
this:
np:hasAssertion
dgn-np:NP411378.RAHVMiE3J7puyUd2B71Z9hlXHseyq4KQ4U2vu2LKJ0_gI130_assertion
;
np:hasProvenance
dgn-np:NP411378.RAHVMiE3J7puyUd2B71Z9hlXHseyq4KQ4U2vu2LKJ0_gI130_provenance
;
np:hasPublicationInfo
dgn-np:NP411378.RAHVMiE3J7puyUd2B71Z9hlXHseyq4KQ4U2vu2LKJ0_gI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP411378.RAHVMiE3J7puyUd2B71Z9hlXHseyq4KQ4U2vu2LKJ0_gI130_assertion
a
np:Assertion
.
dgn-np:NP411378.RAHVMiE3J7puyUd2B71Z9hlXHseyq4KQ4U2vu2LKJ0_gI130_provenance
a
np:Provenance
.
dgn-np:NP411378.RAHVMiE3J7puyUd2B71Z9hlXHseyq4KQ4U2vu2LKJ0_gI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP411378.RAHVMiE3J7puyUd2B71Z9hlXHseyq4KQ4U2vu2LKJ0_gI130_assertion
{
miriam-gene:5728
a
ncit:C16612
.
lld:C1458156
a
ncit:C7057
.
dgn-gda:DGN8d46519ea46841358185fd88aa450e33
sio:SIO_000628
miriam-gene:5728
,
lld:C1458156
;
a
sio:SIO_001121
.
}
dgn-np:NP411378.RAHVMiE3J7puyUd2B71Z9hlXHseyq4KQ4U2vu2LKJ0_gI130_provenance
{
dgn-np:NP411378.RAHVMiE3J7puyUd2B71Z9hlXHseyq4KQ4U2vu2LKJ0_gI130_assertion
dcterms:description
"[Identification of patients with low EGR1 therefore may identify patients at high risk for disease recurrence and may also identify patients who have tumors resistant to therapy secondary to loss of pathways such as PTEN.]. 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:15774784
;
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:NP411378.RAHVMiE3J7puyUd2B71Z9hlXHseyq4KQ4U2vu2LKJ0_gI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:04+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" .
}