@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP752445.RAUCpH_3MYy43Tb5F0138-AWNwuZu_LfFNJfsG4bclUso
> .
@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:NP752445.RAUCpH_3MYy43Tb5F0138-AWNwuZu_LfFNJfsG4bclUso130_head
{
this:
np:hasAssertion
dgn-np:NP752445.RAUCpH_3MYy43Tb5F0138-AWNwuZu_LfFNJfsG4bclUso130_assertion
;
np:hasProvenance
dgn-np:NP752445.RAUCpH_3MYy43Tb5F0138-AWNwuZu_LfFNJfsG4bclUso130_provenance
;
np:hasPublicationInfo
dgn-np:NP752445.RAUCpH_3MYy43Tb5F0138-AWNwuZu_LfFNJfsG4bclUso130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP752445.RAUCpH_3MYy43Tb5F0138-AWNwuZu_LfFNJfsG4bclUso130_assertion
a
np:Assertion
.
dgn-np:NP752445.RAUCpH_3MYy43Tb5F0138-AWNwuZu_LfFNJfsG4bclUso130_provenance
a
np:Provenance
.
dgn-np:NP752445.RAUCpH_3MYy43Tb5F0138-AWNwuZu_LfFNJfsG4bclUso130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP752445.RAUCpH_3MYy43Tb5F0138-AWNwuZu_LfFNJfsG4bclUso130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C0206701
a
ncit:C7057
.
dgn-gda:DGN520c69cfd8f31982295d5d576436842b
sio:SIO_000628
miriam-gene:1956
,
lld:C0206701
;
a
sio:SIO_001121
.
}
dgn-np:NP752445.RAUCpH_3MYy43Tb5F0138-AWNwuZu_LfFNJfsG4bclUso130_provenance
{
dgn-np:NP752445.RAUCpH_3MYy43Tb5F0138-AWNwuZu_LfFNJfsG4bclUso130_assertion
dcterms:description
"[The purpose of this study was to examine the frequency and clinicopathological correlations of gene amplification, protein expression, and mutations of EGFR and ERBB2 in serous carcinoma, the most common and aggressive type of ovarian cancer.]. 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:16607561
;
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:NP752445.RAUCpH_3MYy43Tb5F0138-AWNwuZu_LfFNJfsG4bclUso130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:36+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" .
}