@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP567077.RAG1zeme6uSJ6WGxXrzAY2pV0VTfGmZk2AboV3fiRPWuU
> .
@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:NP567077.RAG1zeme6uSJ6WGxXrzAY2pV0VTfGmZk2AboV3fiRPWuU130_head
{
this:
np:hasAssertion
dgn-np:NP567077.RAG1zeme6uSJ6WGxXrzAY2pV0VTfGmZk2AboV3fiRPWuU130_assertion
;
np:hasProvenance
dgn-np:NP567077.RAG1zeme6uSJ6WGxXrzAY2pV0VTfGmZk2AboV3fiRPWuU130_provenance
;
np:hasPublicationInfo
dgn-np:NP567077.RAG1zeme6uSJ6WGxXrzAY2pV0VTfGmZk2AboV3fiRPWuU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP567077.RAG1zeme6uSJ6WGxXrzAY2pV0VTfGmZk2AboV3fiRPWuU130_assertion
a
np:Assertion
.
dgn-np:NP567077.RAG1zeme6uSJ6WGxXrzAY2pV0VTfGmZk2AboV3fiRPWuU130_provenance
a
np:Provenance
.
dgn-np:NP567077.RAG1zeme6uSJ6WGxXrzAY2pV0VTfGmZk2AboV3fiRPWuU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP567077.RAG1zeme6uSJ6WGxXrzAY2pV0VTfGmZk2AboV3fiRPWuU130_assertion
{
miriam-gene:2463
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGN566b82e3bc4139fe99deccbe76e0c120
sio:SIO_000628
miriam-gene:2463
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP567077.RAG1zeme6uSJ6WGxXrzAY2pV0VTfGmZk2AboV3fiRPWuU130_provenance
{
dgn-np:NP567077.RAG1zeme6uSJ6WGxXrzAY2pV0VTfGmZk2AboV3fiRPWuU130_assertion
dcterms:description
"[The major aim of the present study was to determine whether the FRA16D chromosomal fragile site locus has a role to play in predisposing DNA sequences within and adjacent to the fragile site to DNA instability (such as deletion or translocation), which could lead to or be associated with neoplasia.]. 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:10749140
;
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:NP567077.RAG1zeme6uSJ6WGxXrzAY2pV0VTfGmZk2AboV3fiRPWuU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:42+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" .
}