@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP614083.RAGfO4By7QEY992tnf08KZA9ypfvr63zAm2wDwq5AoKqI
> .
@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:NP614083.RAGfO4By7QEY992tnf08KZA9ypfvr63zAm2wDwq5AoKqI130_head
{
this:
np:hasAssertion
dgn-np:NP614083.RAGfO4By7QEY992tnf08KZA9ypfvr63zAm2wDwq5AoKqI130_assertion
;
np:hasProvenance
dgn-np:NP614083.RAGfO4By7QEY992tnf08KZA9ypfvr63zAm2wDwq5AoKqI130_provenance
;
np:hasPublicationInfo
dgn-np:NP614083.RAGfO4By7QEY992tnf08KZA9ypfvr63zAm2wDwq5AoKqI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP614083.RAGfO4By7QEY992tnf08KZA9ypfvr63zAm2wDwq5AoKqI130_assertion
a
np:Assertion
.
dgn-np:NP614083.RAGfO4By7QEY992tnf08KZA9ypfvr63zAm2wDwq5AoKqI130_provenance
a
np:Provenance
.
dgn-np:NP614083.RAGfO4By7QEY992tnf08KZA9ypfvr63zAm2wDwq5AoKqI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP614083.RAGfO4By7QEY992tnf08KZA9ypfvr63zAm2wDwq5AoKqI130_assertion
{
miriam-gene:9401
a
ncit:C16612
.
lld:C0000768
a
ncit:C7057
.
dgn-gda:DGN7ff00d7e13d9b8ed2ed6988d9747e010
sio:SIO_000628
miriam-gene:9401
,
lld:C0000768
;
a
sio:SIO_001121
.
}
dgn-np:NP614083.RAGfO4By7QEY992tnf08KZA9ypfvr63zAm2wDwq5AoKqI130_provenance
{
dgn-np:NP614083.RAGfO4By7QEY992tnf08KZA9ypfvr63zAm2wDwq5AoKqI130_assertion
dcterms:description
"[Further work is needed to define the specific and shared functions of RECQL4 in relation to other RecQ helicases and to connect RECQL4 diseases to other genomic instability syndromes with birth defects and cancer predisposition.]. 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:16271439
;
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:NP614083.RAGfO4By7QEY992tnf08KZA9ypfvr63zAm2wDwq5AoKqI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:11+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" .
}