@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP418505.RAwpdPaRYNHxOlQgmGL3qPnGk_JrKIHyjLOb9MUeazMzs
> .
@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:NP418505.RAwpdPaRYNHxOlQgmGL3qPnGk_JrKIHyjLOb9MUeazMzs130_head
{
this:
np:hasAssertion
dgn-np:NP418505.RAwpdPaRYNHxOlQgmGL3qPnGk_JrKIHyjLOb9MUeazMzs130_assertion
;
np:hasProvenance
dgn-np:NP418505.RAwpdPaRYNHxOlQgmGL3qPnGk_JrKIHyjLOb9MUeazMzs130_provenance
;
np:hasPublicationInfo
dgn-np:NP418505.RAwpdPaRYNHxOlQgmGL3qPnGk_JrKIHyjLOb9MUeazMzs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP418505.RAwpdPaRYNHxOlQgmGL3qPnGk_JrKIHyjLOb9MUeazMzs130_assertion
a
np:Assertion
.
dgn-np:NP418505.RAwpdPaRYNHxOlQgmGL3qPnGk_JrKIHyjLOb9MUeazMzs130_provenance
a
np:Provenance
.
dgn-np:NP418505.RAwpdPaRYNHxOlQgmGL3qPnGk_JrKIHyjLOb9MUeazMzs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP418505.RAwpdPaRYNHxOlQgmGL3qPnGk_JrKIHyjLOb9MUeazMzs130_assertion
{
miriam-gene:2064
a
ncit:C16612
.
lld:C0795864
a
ncit:C7057
.
dgn-gda:DGNe38bd922fb07698e39f234ffe0d041a3
sio:SIO_000628
miriam-gene:2064
,
lld:C0795864
;
a
sio:SIO_001121
.
}
dgn-np:NP418505.RAwpdPaRYNHxOlQgmGL3qPnGk_JrKIHyjLOb9MUeazMzs130_provenance
{
dgn-np:NP418505.RAwpdPaRYNHxOlQgmGL3qPnGk_JrKIHyjLOb9MUeazMzs130_assertion
dcterms:description
"[Additional FISH studies that use probes to the SMS, RARA, and TP53 genes are an effective way to determine the true HER2 amplification status in patients with polysomy 17 and they have important potential implications for guiding HER2-targeted therapy in breast 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:21947821
;
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:NP418505.RAwpdPaRYNHxOlQgmGL3qPnGk_JrKIHyjLOb9MUeazMzs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:08+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" .
}