@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP221819.RA5tHwC0D3BBJFD85lUICriRZre6CP80FrFIijTigdvSM
> .
@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:NP221819.RA5tHwC0D3BBJFD85lUICriRZre6CP80FrFIijTigdvSM130_head
{
this:
np:hasAssertion
dgn-np:NP221819.RA5tHwC0D3BBJFD85lUICriRZre6CP80FrFIijTigdvSM130_assertion
;
np:hasProvenance
dgn-np:NP221819.RA5tHwC0D3BBJFD85lUICriRZre6CP80FrFIijTigdvSM130_provenance
;
np:hasPublicationInfo
dgn-np:NP221819.RA5tHwC0D3BBJFD85lUICriRZre6CP80FrFIijTigdvSM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP221819.RA5tHwC0D3BBJFD85lUICriRZre6CP80FrFIijTigdvSM130_assertion
a
np:Assertion
.
dgn-np:NP221819.RA5tHwC0D3BBJFD85lUICriRZre6CP80FrFIijTigdvSM130_provenance
a
np:Provenance
.
dgn-np:NP221819.RA5tHwC0D3BBJFD85lUICriRZre6CP80FrFIijTigdvSM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP221819.RA5tHwC0D3BBJFD85lUICriRZre6CP80FrFIijTigdvSM130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C1336076
a
ncit:C7057
.
dgn-gda:DGN613d972a633ec354e3d4544e6ec4f803
sio:SIO_000628
miriam-gene:7157
,
lld:C1336076
;
a
sio:SIO_001121
.
}
dgn-np:NP221819.RA5tHwC0D3BBJFD85lUICriRZre6CP80FrFIijTigdvSM130_provenance
{
dgn-np:NP221819.RA5tHwC0D3BBJFD85lUICriRZre6CP80FrFIijTigdvSM130_assertion
dcterms:description
"[We performed TP53 mutation analysis and genomewide analysis of loss of heterozygosity and allelic imbalance on DNA from isolated neoplastic epithelial and stromal cells from 43 patients with hereditary breast cancer and 175 patients with sporadic 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:18094375
;
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:NP221819.RA5tHwC0D3BBJFD85lUICriRZre6CP80FrFIijTigdvSM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:03+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" .
}