@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP898544.RAFN6weLkETbk69mI3xcyOjT1DvXsvLdZF32q3WNr5MDU
> .
@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:NP898544.RAFN6weLkETbk69mI3xcyOjT1DvXsvLdZF32q3WNr5MDU130_head
{
this:
np:hasAssertion
dgn-np:NP898544.RAFN6weLkETbk69mI3xcyOjT1DvXsvLdZF32q3WNr5MDU130_assertion
;
np:hasProvenance
dgn-np:NP898544.RAFN6weLkETbk69mI3xcyOjT1DvXsvLdZF32q3WNr5MDU130_provenance
;
np:hasPublicationInfo
dgn-np:NP898544.RAFN6weLkETbk69mI3xcyOjT1DvXsvLdZF32q3WNr5MDU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP898544.RAFN6weLkETbk69mI3xcyOjT1DvXsvLdZF32q3WNr5MDU130_assertion
a
np:Assertion
.
dgn-np:NP898544.RAFN6weLkETbk69mI3xcyOjT1DvXsvLdZF32q3WNr5MDU130_provenance
a
np:Provenance
.
dgn-np:NP898544.RAFN6weLkETbk69mI3xcyOjT1DvXsvLdZF32q3WNr5MDU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP898544.RAFN6weLkETbk69mI3xcyOjT1DvXsvLdZF32q3WNr5MDU130_assertion
{
miriam-gene:6624
a
ncit:C16612
.
lld:C0015625
a
ncit:C7057
.
dgn-gda:DGNb5e737bb6df7bde4db9e0163414996bd
sio:SIO_000628
miriam-gene:6624
,
lld:C0015625
;
a
sio:SIO_001121
.
}
dgn-np:NP898544.RAFN6weLkETbk69mI3xcyOjT1DvXsvLdZF32q3WNr5MDU130_provenance
{
dgn-np:NP898544.RAFN6weLkETbk69mI3xcyOjT1DvXsvLdZF32q3WNr5MDU130_assertion
dcterms:description
"[This finding, coupled with evidence showing that DT40 cells deficient in both FAN1 and FANCC, or FAN1 and FANCJ, exhibited increased sensitivity to cisplatin compared with cells lacking only FAN1, suggests that, despite its association with FANCD2/FANCI, FAN1 in DT40 cells participates in the processing of damage induced by interstrand cross-linking-generating agents also independently of the classical FA pathway.]. 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:21115814
;
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:NP898544.RAFN6weLkETbk69mI3xcyOjT1DvXsvLdZF32q3WNr5MDU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:12+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" .
}