@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP441959.RAIIa782wxTNaHn8hCMEMVN-btYllhCLx27MpTp0vfQYo
> .
@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:NP441959.RAIIa782wxTNaHn8hCMEMVN-btYllhCLx27MpTp0vfQYo130_head
{
this:
np:hasAssertion
dgn-np:NP441959.RAIIa782wxTNaHn8hCMEMVN-btYllhCLx27MpTp0vfQYo130_assertion
;
np:hasProvenance
dgn-np:NP441959.RAIIa782wxTNaHn8hCMEMVN-btYllhCLx27MpTp0vfQYo130_provenance
;
np:hasPublicationInfo
dgn-np:NP441959.RAIIa782wxTNaHn8hCMEMVN-btYllhCLx27MpTp0vfQYo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP441959.RAIIa782wxTNaHn8hCMEMVN-btYllhCLx27MpTp0vfQYo130_assertion
a
np:Assertion
.
dgn-np:NP441959.RAIIa782wxTNaHn8hCMEMVN-btYllhCLx27MpTp0vfQYo130_provenance
a
np:Provenance
.
dgn-np:NP441959.RAIIa782wxTNaHn8hCMEMVN-btYllhCLx27MpTp0vfQYo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP441959.RAIIa782wxTNaHn8hCMEMVN-btYllhCLx27MpTp0vfQYo130_assertion
{
miriam-gene:51741
a
ncit:C16612
.
lld:C3469521
a
ncit:C7057
.
dgn-gda:DGN2bdab15fff1c13f67776e9ab3ccfa962
sio:SIO_000628
miriam-gene:51741
,
lld:C3469521
;
a
sio:SIO_001121
.
}
dgn-np:NP441959.RAIIa782wxTNaHn8hCMEMVN-btYllhCLx27MpTp0vfQYo130_provenance
{
dgn-np:NP441959.RAIIa782wxTNaHn8hCMEMVN-btYllhCLx27MpTp0vfQYo130_assertion
dcterms:description
"[Both the total number of chromosome gaps and breaks and breaks at the specific common fragile sites FRA3B and FRA16D were significantly elevated in the absence of an intact 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:15661754
;
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:NP441959.RAIIa782wxTNaHn8hCMEMVN-btYllhCLx27MpTp0vfQYo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:21+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" .
}