@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP221600.RAz5fMO3OK8KmTPTas7a0Zmzz8g52Q4IA65tD8rEo9Dvo
> .
@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:NP221600.RAz5fMO3OK8KmTPTas7a0Zmzz8g52Q4IA65tD8rEo9Dvo130_head
{
this:
np:hasAssertion
dgn-np:NP221600.RAz5fMO3OK8KmTPTas7a0Zmzz8g52Q4IA65tD8rEo9Dvo130_assertion
;
np:hasProvenance
dgn-np:NP221600.RAz5fMO3OK8KmTPTas7a0Zmzz8g52Q4IA65tD8rEo9Dvo130_provenance
;
np:hasPublicationInfo
dgn-np:NP221600.RAz5fMO3OK8KmTPTas7a0Zmzz8g52Q4IA65tD8rEo9Dvo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP221600.RAz5fMO3OK8KmTPTas7a0Zmzz8g52Q4IA65tD8rEo9Dvo130_assertion
a
np:Assertion
.
dgn-np:NP221600.RAz5fMO3OK8KmTPTas7a0Zmzz8g52Q4IA65tD8rEo9Dvo130_provenance
a
np:Provenance
.
dgn-np:NP221600.RAz5fMO3OK8KmTPTas7a0Zmzz8g52Q4IA65tD8rEo9Dvo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP221600.RAz5fMO3OK8KmTPTas7a0Zmzz8g52Q4IA65tD8rEo9Dvo130_assertion
{
miriam-gene:2064
a
ncit:C16612
.
lld:C1883486
a
ncit:C7057
.
dgn-gda:DGN7b161f56a53a0620d6e09f581447e735
sio:SIO_000628
miriam-gene:2064
,
lld:C1883486
;
a
sio:SIO_001121
.
}
dgn-np:NP221600.RAz5fMO3OK8KmTPTas7a0Zmzz8g52Q4IA65tD8rEo9Dvo130_provenance
{
dgn-np:NP221600.RAz5fMO3OK8KmTPTas7a0Zmzz8g52Q4IA65tD8rEo9Dvo130_assertion
dcterms:description
"[Overexpression of HER2/neu in uterine serous papillary endometrial cancer is an independent variable that is associated with poor outcome, occurs more frequently in black women, and may contribute to racial disparity in survival.]. 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:15746676
;
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:NP221600.RAz5fMO3OK8KmTPTas7a0Zmzz8g52Q4IA65tD8rEo9Dvo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:03+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" .
}