@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP263668.RADeI2UHjIbRfwb9Px0gpOnXMAPdJrVzDBvG7juvFZmsQ
> .
@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:NP263668.RADeI2UHjIbRfwb9Px0gpOnXMAPdJrVzDBvG7juvFZmsQ130_head
{
this:
np:hasAssertion
dgn-np:NP263668.RADeI2UHjIbRfwb9Px0gpOnXMAPdJrVzDBvG7juvFZmsQ130_assertion
;
np:hasProvenance
dgn-np:NP263668.RADeI2UHjIbRfwb9Px0gpOnXMAPdJrVzDBvG7juvFZmsQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP263668.RADeI2UHjIbRfwb9Px0gpOnXMAPdJrVzDBvG7juvFZmsQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP263668.RADeI2UHjIbRfwb9Px0gpOnXMAPdJrVzDBvG7juvFZmsQ130_assertion
a
np:Assertion
.
dgn-np:NP263668.RADeI2UHjIbRfwb9Px0gpOnXMAPdJrVzDBvG7juvFZmsQ130_provenance
a
np:Provenance
.
dgn-np:NP263668.RADeI2UHjIbRfwb9Px0gpOnXMAPdJrVzDBvG7juvFZmsQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP263668.RADeI2UHjIbRfwb9Px0gpOnXMAPdJrVzDBvG7juvFZmsQ130_assertion
{
miriam-gene:2272
a
ncit:C16612
.
lld:C0149925
a
ncit:C7057
.
dgn-gda:DGNf5a9c7432af5f514e7e3830a24728281
sio:SIO_000628
miriam-gene:2272
,
lld:C0149925
;
a
sio:SIO_001121
.
}
dgn-np:NP263668.RADeI2UHjIbRfwb9Px0gpOnXMAPdJrVzDBvG7juvFZmsQ130_provenance
{
dgn-np:NP263668.RADeI2UHjIbRfwb9Px0gpOnXMAPdJrVzDBvG7juvFZmsQ130_assertion
dcterms:description
"[To determine whether some individuals have increased fragility of FRA3B that might increase the risk for breakage or deletion in 3p14.2, fragile site expression was examined in smokers, nonsmokers, and small cell lung cancer (SCLC) patients.]. 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:12007194
;
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:NP263668.RADeI2UHjIbRfwb9Px0gpOnXMAPdJrVzDBvG7juvFZmsQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:27+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" .
}