@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP315362.RAxNhoxAq9i0jOKrFyvdRebCa2r8Bba1lgFeVXtO3Xz3E
> .
@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:NP315362.RAxNhoxAq9i0jOKrFyvdRebCa2r8Bba1lgFeVXtO3Xz3E130_head
{
this:
np:hasAssertion
dgn-np:NP315362.RAxNhoxAq9i0jOKrFyvdRebCa2r8Bba1lgFeVXtO3Xz3E130_assertion
;
np:hasProvenance
dgn-np:NP315362.RAxNhoxAq9i0jOKrFyvdRebCa2r8Bba1lgFeVXtO3Xz3E130_provenance
;
np:hasPublicationInfo
dgn-np:NP315362.RAxNhoxAq9i0jOKrFyvdRebCa2r8Bba1lgFeVXtO3Xz3E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP315362.RAxNhoxAq9i0jOKrFyvdRebCa2r8Bba1lgFeVXtO3Xz3E130_assertion
a
np:Assertion
.
dgn-np:NP315362.RAxNhoxAq9i0jOKrFyvdRebCa2r8Bba1lgFeVXtO3Xz3E130_provenance
a
np:Provenance
.
dgn-np:NP315362.RAxNhoxAq9i0jOKrFyvdRebCa2r8Bba1lgFeVXtO3Xz3E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP315362.RAxNhoxAq9i0jOKrFyvdRebCa2r8Bba1lgFeVXtO3Xz3E130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C1140680
a
ncit:C7057
.
dgn-gda:DGNf0a571bc703aa70a55554888fc1dd00e
sio:SIO_000628
miriam-gene:1956
,
lld:C1140680
;
a
sio:SIO_001121
.
}
dgn-np:NP315362.RAxNhoxAq9i0jOKrFyvdRebCa2r8Bba1lgFeVXtO3Xz3E130_provenance
{
dgn-np:NP315362.RAxNhoxAq9i0jOKrFyvdRebCa2r8Bba1lgFeVXtO3Xz3E130_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:NP315362.RAxNhoxAq9i0jOKrFyvdRebCa2r8Bba1lgFeVXtO3Xz3E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:00+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" .
}