@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP535764.RAyNI_8v2-1wl_laEIyx2MyR4jcOShG2LJmM1mhytq_Tk
> .
@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:NP535764.RAyNI_8v2-1wl_laEIyx2MyR4jcOShG2LJmM1mhytq_Tk130_head
{
this:
np:hasAssertion
dgn-np:NP535764.RAyNI_8v2-1wl_laEIyx2MyR4jcOShG2LJmM1mhytq_Tk130_assertion
;
np:hasProvenance
dgn-np:NP535764.RAyNI_8v2-1wl_laEIyx2MyR4jcOShG2LJmM1mhytq_Tk130_provenance
;
np:hasPublicationInfo
dgn-np:NP535764.RAyNI_8v2-1wl_laEIyx2MyR4jcOShG2LJmM1mhytq_Tk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP535764.RAyNI_8v2-1wl_laEIyx2MyR4jcOShG2LJmM1mhytq_Tk130_assertion
a
np:Assertion
.
dgn-np:NP535764.RAyNI_8v2-1wl_laEIyx2MyR4jcOShG2LJmM1mhytq_Tk130_provenance
a
np:Provenance
.
dgn-np:NP535764.RAyNI_8v2-1wl_laEIyx2MyR4jcOShG2LJmM1mhytq_Tk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP535764.RAyNI_8v2-1wl_laEIyx2MyR4jcOShG2LJmM1mhytq_Tk130_assertion
{
miriam-gene:6624
a
ncit:C16612
.
lld:C3469521
a
ncit:C7057
.
dgn-gda:DGN8d0f6a86f6ec76d620ef3534625b4414
sio:SIO_000628
miriam-gene:6624
,
lld:C3469521
;
a
sio:SIO_001121
.
}
dgn-np:NP535764.RAyNI_8v2-1wl_laEIyx2MyR4jcOShG2LJmM1mhytq_Tk130_provenance
{
dgn-np:NP535764.RAyNI_8v2-1wl_laEIyx2MyR4jcOShG2LJmM1mhytq_Tk130_assertion
dcterms:description
"[A candidate protein for those patients, FA nuclease 1 (FAN1), whose gene is located at chromosome 15q13.3, is recruited to stalled replication forks by binding to monoubiquitinated FANCD2 and is required for interstrand crosslink repair, suggesting that mutation of FAN1 may cause FA.]. 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:22611161
;
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:NP535764.RAyNI_8v2-1wl_laEIyx2MyR4jcOShG2LJmM1mhytq_Tk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:23+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" .
}