@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP339081.RAKkVFhb_h9M8CPfSr3ovhPYSDnfKLUf79qoOLKMTsY6g
> .
@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:NP339081.RAKkVFhb_h9M8CPfSr3ovhPYSDnfKLUf79qoOLKMTsY6g130_head
{
this:
np:hasAssertion
dgn-np:NP339081.RAKkVFhb_h9M8CPfSr3ovhPYSDnfKLUf79qoOLKMTsY6g130_assertion
;
np:hasProvenance
dgn-np:NP339081.RAKkVFhb_h9M8CPfSr3ovhPYSDnfKLUf79qoOLKMTsY6g130_provenance
;
np:hasPublicationInfo
dgn-np:NP339081.RAKkVFhb_h9M8CPfSr3ovhPYSDnfKLUf79qoOLKMTsY6g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP339081.RAKkVFhb_h9M8CPfSr3ovhPYSDnfKLUf79qoOLKMTsY6g130_assertion
a
np:Assertion
.
dgn-np:NP339081.RAKkVFhb_h9M8CPfSr3ovhPYSDnfKLUf79qoOLKMTsY6g130_provenance
a
np:Provenance
.
dgn-np:NP339081.RAKkVFhb_h9M8CPfSr3ovhPYSDnfKLUf79qoOLKMTsY6g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP339081.RAKkVFhb_h9M8CPfSr3ovhPYSDnfKLUf79qoOLKMTsY6g130_assertion
{
miriam-gene:2178
a
ncit:C16612
.
lld:C0015625
a
ncit:C7057
.
dgn-gda:DGN09232d3993f547533fa538ef43433618
sio:SIO_000628
miriam-gene:2178
,
lld:C0015625
;
a
sio:SIO_001121
.
}
dgn-np:NP339081.RAKkVFhb_h9M8CPfSr3ovhPYSDnfKLUf79qoOLKMTsY6g130_provenance
{
dgn-np:NP339081.RAKkVFhb_h9M8CPfSr3ovhPYSDnfKLUf79qoOLKMTsY6g130_assertion
dcterms:description
"[This pathway regulates cisplatin sensitivity and is governed by the coordinate activity of six genes associated with Fanconi anemia (FANCA, FANCC, FANCD2, FANCE, FANCF and FANCG) as well as BRCA1 and BRCA2 (FANCD1).]. 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:12692539
;
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:NP339081.RAKkVFhb_h9M8CPfSr3ovhPYSDnfKLUf79qoOLKMTsY6g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:19+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" .
}