@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP389079.RAYRDa794l3BFeM_h7oZmjq1Gx0EV63oUxM90iPdeuR5c
> .
@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:NP389079.RAYRDa794l3BFeM_h7oZmjq1Gx0EV63oUxM90iPdeuR5c130_head
{
this:
np:hasAssertion
dgn-np:NP389079.RAYRDa794l3BFeM_h7oZmjq1Gx0EV63oUxM90iPdeuR5c130_assertion
;
np:hasProvenance
dgn-np:NP389079.RAYRDa794l3BFeM_h7oZmjq1Gx0EV63oUxM90iPdeuR5c130_provenance
;
np:hasPublicationInfo
dgn-np:NP389079.RAYRDa794l3BFeM_h7oZmjq1Gx0EV63oUxM90iPdeuR5c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP389079.RAYRDa794l3BFeM_h7oZmjq1Gx0EV63oUxM90iPdeuR5c130_assertion
a
np:Assertion
.
dgn-np:NP389079.RAYRDa794l3BFeM_h7oZmjq1Gx0EV63oUxM90iPdeuR5c130_provenance
a
np:Provenance
.
dgn-np:NP389079.RAYRDa794l3BFeM_h7oZmjq1Gx0EV63oUxM90iPdeuR5c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP389079.RAYRDa794l3BFeM_h7oZmjq1Gx0EV63oUxM90iPdeuR5c130_assertion
{
miriam-gene:2099
a
ncit:C16612
.
lld:C1262091
a
ncit:C7057
.
dgn-gda:DGN66ce44e0ebb8c1db0c660ba367bf8829
sio:SIO_000628
miriam-gene:2099
,
lld:C1262091
;
a
sio:SIO_001121
.
}
dgn-np:NP389079.RAYRDa794l3BFeM_h7oZmjq1Gx0EV63oUxM90iPdeuR5c130_provenance
{
dgn-np:NP389079.RAYRDa794l3BFeM_h7oZmjq1Gx0EV63oUxM90iPdeuR5c130_assertion
dcterms:description
"[In addition, high ER mRNA levels were associated with absence or minimal necrosis and vascular invasion together with absence or minimal level of tumor lymphocytic infiltration, but not with age, clinical stage, tumor size or overexpression of c-myc or c-erbB-2 mRNA.]. 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:7927940
;
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:NP389079.RAYRDa794l3BFeM_h7oZmjq1Gx0EV63oUxM90iPdeuR5c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:52+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" .
}