@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP888640.RAprbYFJBMPAjhqgj8UCT4VgOUivwddv_rJNoGlyv4w4I
> .
@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:NP888640.RAprbYFJBMPAjhqgj8UCT4VgOUivwddv_rJNoGlyv4w4I130_head
{
this:
np:hasAssertion
dgn-np:NP888640.RAprbYFJBMPAjhqgj8UCT4VgOUivwddv_rJNoGlyv4w4I130_assertion
;
np:hasProvenance
dgn-np:NP888640.RAprbYFJBMPAjhqgj8UCT4VgOUivwddv_rJNoGlyv4w4I130_provenance
;
np:hasPublicationInfo
dgn-np:NP888640.RAprbYFJBMPAjhqgj8UCT4VgOUivwddv_rJNoGlyv4w4I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP888640.RAprbYFJBMPAjhqgj8UCT4VgOUivwddv_rJNoGlyv4w4I130_assertion
a
np:Assertion
.
dgn-np:NP888640.RAprbYFJBMPAjhqgj8UCT4VgOUivwddv_rJNoGlyv4w4I130_provenance
a
np:Provenance
.
dgn-np:NP888640.RAprbYFJBMPAjhqgj8UCT4VgOUivwddv_rJNoGlyv4w4I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP888640.RAprbYFJBMPAjhqgj8UCT4VgOUivwddv_rJNoGlyv4w4I130_assertion
{
miriam-gene:57045
a
ncit:C16612
.
lld:C0684249
a
ncit:C7057
.
dgn-gda:DGN2c427059b50ff73449a83e53e63e27ec
sio:SIO_000628
miriam-gene:57045
,
lld:C0684249
;
a
sio:SIO_001121
.
}
dgn-np:NP888640.RAprbYFJBMPAjhqgj8UCT4VgOUivwddv_rJNoGlyv4w4I130_provenance
{
dgn-np:NP888640.RAprbYFJBMPAjhqgj8UCT4VgOUivwddv_rJNoGlyv4w4I130_assertion
dcterms:description
"[The smallest region homozygously deleted in 3p21.3C was located between D3S1568 (CACNA2D2 gene) and D3S4604 (SEMA3F gene) and contains 17 genes previously defined as lung cancer candidate Tumor suppressor genes (TSG(s)).]. 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:12771950
;
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:NP888640.RAprbYFJBMPAjhqgj8UCT4VgOUivwddv_rJNoGlyv4w4I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:06+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: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" .
}