@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP343095.RAVx6po3Rn0JSLy8T_WBt4DMi8bwfr2_y-JXMFqNRkPpY
> .
@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:NP343095.RAVx6po3Rn0JSLy8T_WBt4DMi8bwfr2_y-JXMFqNRkPpY130_head
{
this:
np:hasAssertion
dgn-np:NP343095.RAVx6po3Rn0JSLy8T_WBt4DMi8bwfr2_y-JXMFqNRkPpY130_assertion
;
np:hasProvenance
dgn-np:NP343095.RAVx6po3Rn0JSLy8T_WBt4DMi8bwfr2_y-JXMFqNRkPpY130_provenance
;
np:hasPublicationInfo
dgn-np:NP343095.RAVx6po3Rn0JSLy8T_WBt4DMi8bwfr2_y-JXMFqNRkPpY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP343095.RAVx6po3Rn0JSLy8T_WBt4DMi8bwfr2_y-JXMFqNRkPpY130_assertion
a
np:Assertion
.
dgn-np:NP343095.RAVx6po3Rn0JSLy8T_WBt4DMi8bwfr2_y-JXMFqNRkPpY130_provenance
a
np:Provenance
.
dgn-np:NP343095.RAVx6po3Rn0JSLy8T_WBt4DMi8bwfr2_y-JXMFqNRkPpY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP343095.RAVx6po3Rn0JSLy8T_WBt4DMi8bwfr2_y-JXMFqNRkPpY130_assertion
{
miriam-gene:57508
a
ncit:C16612
.
lld:C1458155
a
ncit:C7057
.
dgn-gda:DGNf0443d4c2b4cb9125cc1c51f57a8bb31
sio:SIO_000628
miriam-gene:57508
,
lld:C1458155
;
a
sio:SIO_001121
.
}
dgn-np:NP343095.RAVx6po3Rn0JSLy8T_WBt4DMi8bwfr2_y-JXMFqNRkPpY130_provenance
{
dgn-np:NP343095.RAVx6po3Rn0JSLy8T_WBt4DMi8bwfr2_y-JXMFqNRkPpY130_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:NP343095.RAVx6po3Rn0JSLy8T_WBt4DMi8bwfr2_y-JXMFqNRkPpY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:22+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" .
}