@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP503132.RAcp9KRbb45NlOAG6WZGCLtcwp2FsffhRxFOhDqPeNKfg
> .
@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:NP503132.RAcp9KRbb45NlOAG6WZGCLtcwp2FsffhRxFOhDqPeNKfg130_head
{
this:
np:hasAssertion
dgn-np:NP503132.RAcp9KRbb45NlOAG6WZGCLtcwp2FsffhRxFOhDqPeNKfg130_assertion
;
np:hasProvenance
dgn-np:NP503132.RAcp9KRbb45NlOAG6WZGCLtcwp2FsffhRxFOhDqPeNKfg130_provenance
;
np:hasPublicationInfo
dgn-np:NP503132.RAcp9KRbb45NlOAG6WZGCLtcwp2FsffhRxFOhDqPeNKfg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP503132.RAcp9KRbb45NlOAG6WZGCLtcwp2FsffhRxFOhDqPeNKfg130_assertion
a
np:Assertion
.
dgn-np:NP503132.RAcp9KRbb45NlOAG6WZGCLtcwp2FsffhRxFOhDqPeNKfg130_provenance
a
np:Provenance
.
dgn-np:NP503132.RAcp9KRbb45NlOAG6WZGCLtcwp2FsffhRxFOhDqPeNKfg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP503132.RAcp9KRbb45NlOAG6WZGCLtcwp2FsffhRxFOhDqPeNKfg130_assertion
{
miriam-gene:2065
a
ncit:C16612
.
lld:C1457883
a
ncit:C7057
.
dgn-gda:DGNeb67b25497803eeede861bb410873285
sio:SIO_000628
miriam-gene:2065
,
lld:C1457883
;
a
sio:SIO_001121
.
}
dgn-np:NP503132.RAcp9KRbb45NlOAG6WZGCLtcwp2FsffhRxFOhDqPeNKfg130_provenance
{
dgn-np:NP503132.RAcp9KRbb45NlOAG6WZGCLtcwp2FsffhRxFOhDqPeNKfg130_assertion
dcterms:description
"[HER2 signalling by heterodimerisation with EGFR and HER3 in breast cancer is associated with worst outcome of the afflicted patients, which is attributed not only to the aggressiveness of such tumours but also to therapy resistance.]. 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:22262199
;
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:NP503132.RAcp9KRbb45NlOAG6WZGCLtcwp2FsffhRxFOhDqPeNKfg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:00+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" .
}