@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP854048.RAjcLwb7FiQIKjSqSvGHoXb_rQRv9X3LMvE3fusBr5Et8
> .
@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:NP854048.RAjcLwb7FiQIKjSqSvGHoXb_rQRv9X3LMvE3fusBr5Et8130_head
{
this:
np:hasAssertion
dgn-np:NP854048.RAjcLwb7FiQIKjSqSvGHoXb_rQRv9X3LMvE3fusBr5Et8130_assertion
;
np:hasProvenance
dgn-np:NP854048.RAjcLwb7FiQIKjSqSvGHoXb_rQRv9X3LMvE3fusBr5Et8130_provenance
;
np:hasPublicationInfo
dgn-np:NP854048.RAjcLwb7FiQIKjSqSvGHoXb_rQRv9X3LMvE3fusBr5Et8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP854048.RAjcLwb7FiQIKjSqSvGHoXb_rQRv9X3LMvE3fusBr5Et8130_assertion
a
np:Assertion
.
dgn-np:NP854048.RAjcLwb7FiQIKjSqSvGHoXb_rQRv9X3LMvE3fusBr5Et8130_provenance
a
np:Provenance
.
dgn-np:NP854048.RAjcLwb7FiQIKjSqSvGHoXb_rQRv9X3LMvE3fusBr5Et8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP854048.RAjcLwb7FiQIKjSqSvGHoXb_rQRv9X3LMvE3fusBr5Et8130_assertion
{
miriam-gene:2248
a
ncit:C16612
.
lld:C1458155
a
ncit:C7057
.
dgn-gda:DGN09aadba2b450b021ee9ad99e97b31d6d
sio:SIO_000628
miriam-gene:2248
,
lld:C1458155
;
a
sio:SIO_001121
.
}
dgn-np:NP854048.RAjcLwb7FiQIKjSqSvGHoXb_rQRv9X3LMvE3fusBr5Et8130_provenance
{
dgn-np:NP854048.RAjcLwb7FiQIKjSqSvGHoXb_rQRv9X3LMvE3fusBr5Et8130_assertion
dcterms:description
"[The authors examined several loci (ERBB2, INT2, MUC1) for gene amplification or loss of heterozygosity by Southern blotting and for gene expression by immunohistochemistry in breast tumors from patient groups selected by survival.]. 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:1355402
;
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:NP854048.RAjcLwb7FiQIKjSqSvGHoXb_rQRv9X3LMvE3fusBr5Et8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:42+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" .
}