@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP508918.RAKGpEp8bLuYLN04Jvf238XslewkzXHid5fOBGYwT5FiQ
> .
@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:NP508918.RAKGpEp8bLuYLN04Jvf238XslewkzXHid5fOBGYwT5FiQ130_head
{
this:
np:hasAssertion
dgn-np:NP508918.RAKGpEp8bLuYLN04Jvf238XslewkzXHid5fOBGYwT5FiQ130_assertion
;
np:hasProvenance
dgn-np:NP508918.RAKGpEp8bLuYLN04Jvf238XslewkzXHid5fOBGYwT5FiQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP508918.RAKGpEp8bLuYLN04Jvf238XslewkzXHid5fOBGYwT5FiQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP508918.RAKGpEp8bLuYLN04Jvf238XslewkzXHid5fOBGYwT5FiQ130_assertion
a
np:Assertion
.
dgn-np:NP508918.RAKGpEp8bLuYLN04Jvf238XslewkzXHid5fOBGYwT5FiQ130_provenance
a
np:Provenance
.
dgn-np:NP508918.RAKGpEp8bLuYLN04Jvf238XslewkzXHid5fOBGYwT5FiQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP508918.RAKGpEp8bLuYLN04Jvf238XslewkzXHid5fOBGYwT5FiQ130_assertion
{
miriam-gene:161003
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGN8c150405e3bbc02a0da78db46a9a8abb
sio:SIO_000628
miriam-gene:161003
,
lld:C0376358
;
a
sio:SIO_001121
.
}
dgn-np:NP508918.RAKGpEp8bLuYLN04Jvf238XslewkzXHid5fOBGYwT5FiQ130_provenance
{
dgn-np:NP508918.RAKGpEp8bLuYLN04Jvf238XslewkzXHid5fOBGYwT5FiQ130_assertion
dcterms:description
"[To narrow down their localization, several loss of heterozygosity (LOH) studies of chromosome arm 16q in sporadic breast and prostate cancers have been carried out to define the most recurrent and smallest region(s) of overlap (SRO) for commonly deleted chromosome arm 16q material.]. 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:9591631
;
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:NP508918.RAKGpEp8bLuYLN04Jvf238XslewkzXHid5fOBGYwT5FiQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:03+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" .
}