@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP403031.RA568LzGSS1TbJf2xel7ykLyrbIwiY_VVQwvZG8LIPs1g
> .
@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:NP403031.RA568LzGSS1TbJf2xel7ykLyrbIwiY_VVQwvZG8LIPs1g130_head
{
this:
np:hasAssertion
dgn-np:NP403031.RA568LzGSS1TbJf2xel7ykLyrbIwiY_VVQwvZG8LIPs1g130_assertion
;
np:hasProvenance
dgn-np:NP403031.RA568LzGSS1TbJf2xel7ykLyrbIwiY_VVQwvZG8LIPs1g130_provenance
;
np:hasPublicationInfo
dgn-np:NP403031.RA568LzGSS1TbJf2xel7ykLyrbIwiY_VVQwvZG8LIPs1g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP403031.RA568LzGSS1TbJf2xel7ykLyrbIwiY_VVQwvZG8LIPs1g130_assertion
a
np:Assertion
.
dgn-np:NP403031.RA568LzGSS1TbJf2xel7ykLyrbIwiY_VVQwvZG8LIPs1g130_provenance
a
np:Provenance
.
dgn-np:NP403031.RA568LzGSS1TbJf2xel7ykLyrbIwiY_VVQwvZG8LIPs1g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP403031.RA568LzGSS1TbJf2xel7ykLyrbIwiY_VVQwvZG8LIPs1g130_assertion
{
miriam-gene:2272
a
ncit:C16612
.
lld:C0149925
a
ncit:C7057
.
dgn-gda:DGN1aec0bb99577034519447d142f4029cc
sio:SIO_000628
miriam-gene:2272
,
lld:C0149925
;
a
sio:SIO_001121
.
}
dgn-np:NP403031.RA568LzGSS1TbJf2xel7ykLyrbIwiY_VVQwvZG8LIPs1g130_provenance
{
dgn-np:NP403031.RA568LzGSS1TbJf2xel7ykLyrbIwiY_VVQwvZG8LIPs1g130_assertion
dcterms:description
"[The common fragile site at 3p14(FRA3B) is cytogenetically close to the positions of translocation and deletion breakpoints frequently observed in renal cell carcinoma (RCC) and small cell carcinoma of the lung.]. 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:3125959
;
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:NP403031.RA568LzGSS1TbJf2xel7ykLyrbIwiY_VVQwvZG8LIPs1g130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:34+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" .
}