@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP257388.RAYPcoRWZBu7sFs8Jyh7f9sHiqYgvku3BZjbrt4_YN6pQ
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP257388.RAYPcoRWZBu7sFs8Jyh7f9sHiqYgvku3BZjbrt4_YN6pQ130_head
{
this:
np:hasAssertion
dgn-np:NP257388.RAYPcoRWZBu7sFs8Jyh7f9sHiqYgvku3BZjbrt4_YN6pQ130_assertion
;
np:hasProvenance
dgn-np:NP257388.RAYPcoRWZBu7sFs8Jyh7f9sHiqYgvku3BZjbrt4_YN6pQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP257388.RAYPcoRWZBu7sFs8Jyh7f9sHiqYgvku3BZjbrt4_YN6pQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP257388.RAYPcoRWZBu7sFs8Jyh7f9sHiqYgvku3BZjbrt4_YN6pQ130_assertion
a
np:Assertion
.
dgn-np:NP257388.RAYPcoRWZBu7sFs8Jyh7f9sHiqYgvku3BZjbrt4_YN6pQ130_provenance
a
np:Provenance
.
dgn-np:NP257388.RAYPcoRWZBu7sFs8Jyh7f9sHiqYgvku3BZjbrt4_YN6pQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP257388.RAYPcoRWZBu7sFs8Jyh7f9sHiqYgvku3BZjbrt4_YN6pQ130_assertion
{
miriam-gene:545
a
ncit:C16612
.
lld:C0567439
a
ncit:C7057
.
dgn-gda:DGN7fd0e52a88d866361aad510f1cafcf4a
sio:SIO_000628
miriam-gene:545
,
lld:C0567439
;
a
sio:SIO_001121
.
}
dgn-np:NP257388.RAYPcoRWZBu7sFs8Jyh7f9sHiqYgvku3BZjbrt4_YN6pQ130_provenance
{
dgn-np:NP257388.RAYPcoRWZBu7sFs8Jyh7f9sHiqYgvku3BZjbrt4_YN6pQ130_assertion
dcterms:description
"[This is the first human genetic syndrome associated with increased chromosome instability at fragile sites following replication stress, and these findings may be related to the phenotypic findings in patients with SCKL1.]. 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:15309689
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP257388.RAYPcoRWZBu7sFs8Jyh7f9sHiqYgvku3BZjbrt4_YN6pQ130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:40:06+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}