@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP195724.RA_yuXZZT35kAO1NEjD0H6KRtYFUl9nwrVAM-484mo3oM
> .
@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:NP195724.RA_yuXZZT35kAO1NEjD0H6KRtYFUl9nwrVAM-484mo3oM130_head
{
this:
np:hasAssertion
dgn-np:NP195724.RA_yuXZZT35kAO1NEjD0H6KRtYFUl9nwrVAM-484mo3oM130_assertion
;
np:hasProvenance
dgn-np:NP195724.RA_yuXZZT35kAO1NEjD0H6KRtYFUl9nwrVAM-484mo3oM130_provenance
;
np:hasPublicationInfo
dgn-np:NP195724.RA_yuXZZT35kAO1NEjD0H6KRtYFUl9nwrVAM-484mo3oM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP195724.RA_yuXZZT35kAO1NEjD0H6KRtYFUl9nwrVAM-484mo3oM130_assertion
a
np:Assertion
.
dgn-np:NP195724.RA_yuXZZT35kAO1NEjD0H6KRtYFUl9nwrVAM-484mo3oM130_provenance
a
np:Provenance
.
dgn-np:NP195724.RA_yuXZZT35kAO1NEjD0H6KRtYFUl9nwrVAM-484mo3oM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP195724.RA_yuXZZT35kAO1NEjD0H6KRtYFUl9nwrVAM-484mo3oM130_assertion
{
miriam-gene:2177
a
ncit:C16612
.
lld:C3469521
a
ncit:C7057
.
dgn-gda:DGN548bec54dc9c3317ef1d8c71923582b1
sio:SIO_000628
miriam-gene:2177
,
lld:C3469521
;
a
sio:SIO_001121
.
}
dgn-np:NP195724.RA_yuXZZT35kAO1NEjD0H6KRtYFUl9nwrVAM-484mo3oM130_provenance
{
dgn-np:NP195724.RA_yuXZZT35kAO1NEjD0H6KRtYFUl9nwrVAM-484mo3oM130_assertion
dcterms:description
"[In conclusion, we established the downstream FA genes FANCD2 and BRCA2 to represent particularly vulnerable parts of the FA pathway, providing direct evidence for the paradoxical assumption that their inactivation could be predominantly selected against in cancer cells.]. 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:17387268
;
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:NP195724.RA_yuXZZT35kAO1NEjD0H6KRtYFUl9nwrVAM-484mo3oM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:47+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" .
}