@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP193935.RAXAkYFh3GAtuQT0b7eakZ5LGbM0l5KbeyydGMPawbrZ8
> .
@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:NP193935.RAXAkYFh3GAtuQT0b7eakZ5LGbM0l5KbeyydGMPawbrZ8130_head
{
this:
np:hasAssertion
dgn-np:NP193935.RAXAkYFh3GAtuQT0b7eakZ5LGbM0l5KbeyydGMPawbrZ8130_assertion
;
np:hasProvenance
dgn-np:NP193935.RAXAkYFh3GAtuQT0b7eakZ5LGbM0l5KbeyydGMPawbrZ8130_provenance
;
np:hasPublicationInfo
dgn-np:NP193935.RAXAkYFh3GAtuQT0b7eakZ5LGbM0l5KbeyydGMPawbrZ8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP193935.RAXAkYFh3GAtuQT0b7eakZ5LGbM0l5KbeyydGMPawbrZ8130_assertion
a
np:Assertion
.
dgn-np:NP193935.RAXAkYFh3GAtuQT0b7eakZ5LGbM0l5KbeyydGMPawbrZ8130_provenance
a
np:Provenance
.
dgn-np:NP193935.RAXAkYFh3GAtuQT0b7eakZ5LGbM0l5KbeyydGMPawbrZ8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP193935.RAXAkYFh3GAtuQT0b7eakZ5LGbM0l5KbeyydGMPawbrZ8130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0242596
a
ncit:C7057
.
dgn-gda:DGNca936c5c752d7035ffa14f119080828a
sio:SIO_000628
miriam-gene:7157
,
lld:C0242596
;
a
sio:SIO_001121
.
}
dgn-np:NP193935.RAXAkYFh3GAtuQT0b7eakZ5LGbM0l5KbeyydGMPawbrZ8130_provenance
{
dgn-np:NP193935.RAXAkYFh3GAtuQT0b7eakZ5LGbM0l5KbeyydGMPawbrZ8130_assertion
dcterms:description
"[The feasibility of applying heterogeneous single base genetic changes as tumour specific markers to detect minimal residual disease in PBPC harvests was studied, using the p53 gene and breast cancer as models.]. 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:12032228
;
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:NP193935.RAXAkYFh3GAtuQT0b7eakZ5LGbM0l5KbeyydGMPawbrZ8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:46+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" .
}