@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP928201.RAkU27DwYoDTdw2zRCM7NO6a5V3tifNyOL40wG4PfIr_k
> .
@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:NP928201.RAkU27DwYoDTdw2zRCM7NO6a5V3tifNyOL40wG4PfIr_k130_head
{
this:
np:hasAssertion
dgn-np:NP928201.RAkU27DwYoDTdw2zRCM7NO6a5V3tifNyOL40wG4PfIr_k130_assertion
;
np:hasProvenance
dgn-np:NP928201.RAkU27DwYoDTdw2zRCM7NO6a5V3tifNyOL40wG4PfIr_k130_provenance
;
np:hasPublicationInfo
dgn-np:NP928201.RAkU27DwYoDTdw2zRCM7NO6a5V3tifNyOL40wG4PfIr_k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP928201.RAkU27DwYoDTdw2zRCM7NO6a5V3tifNyOL40wG4PfIr_k130_assertion
a
np:Assertion
.
dgn-np:NP928201.RAkU27DwYoDTdw2zRCM7NO6a5V3tifNyOL40wG4PfIr_k130_provenance
a
np:Provenance
.
dgn-np:NP928201.RAkU27DwYoDTdw2zRCM7NO6a5V3tifNyOL40wG4PfIr_k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP928201.RAkU27DwYoDTdw2zRCM7NO6a5V3tifNyOL40wG4PfIr_k130_assertion
{
miriam-gene:4830
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGN34221427b0dda58a59fdd68b604ae421
sio:SIO_000628
miriam-gene:4830
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP928201.RAkU27DwYoDTdw2zRCM7NO6a5V3tifNyOL40wG4PfIr_k130_provenance
{
dgn-np:NP928201.RAkU27DwYoDTdw2zRCM7NO6a5V3tifNyOL40wG4PfIr_k130_assertion
dcterms:description
"[To study genetic alterations related to the development and/or progression of breast carcinoma, we examined amplification of the ERBB2, INT2, and MYC genes, as well as loss of heterozygosity (LOH) at loci on 11p, 16q, 17p (D17S5 and TP53), 17q (D17S74 and NME1), and 18q by restriction fragment length polymorphism analysis.]. 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:7903963
;
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:NP928201.RAkU27DwYoDTdw2zRCM7NO6a5V3tifNyOL40wG4PfIr_k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:29+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" .
}