@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP581504.RASkwNmEeEbqA2qLtanETbzkD9vOjpIaE87dnZVLlSlSs
> .
@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:NP581504.RASkwNmEeEbqA2qLtanETbzkD9vOjpIaE87dnZVLlSlSs130_head
{
this:
np:hasAssertion
dgn-np:NP581504.RASkwNmEeEbqA2qLtanETbzkD9vOjpIaE87dnZVLlSlSs130_assertion
;
np:hasProvenance
dgn-np:NP581504.RASkwNmEeEbqA2qLtanETbzkD9vOjpIaE87dnZVLlSlSs130_provenance
;
np:hasPublicationInfo
dgn-np:NP581504.RASkwNmEeEbqA2qLtanETbzkD9vOjpIaE87dnZVLlSlSs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP581504.RASkwNmEeEbqA2qLtanETbzkD9vOjpIaE87dnZVLlSlSs130_assertion
a
np:Assertion
.
dgn-np:NP581504.RASkwNmEeEbqA2qLtanETbzkD9vOjpIaE87dnZVLlSlSs130_provenance
a
np:Provenance
.
dgn-np:NP581504.RASkwNmEeEbqA2qLtanETbzkD9vOjpIaE87dnZVLlSlSs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP581504.RASkwNmEeEbqA2qLtanETbzkD9vOjpIaE87dnZVLlSlSs130_assertion
{
miriam-gene:6280
a
ncit:C16612
.
lld:C0007097
a
ncit:C7057
.
dgn-gda:DGN753574605e977be0ab14f43d3c54d110
sio:SIO_000628
miriam-gene:6280
,
lld:C0007097
;
a
sio:SIO_001121
.
}
dgn-np:NP581504.RASkwNmEeEbqA2qLtanETbzkD9vOjpIaE87dnZVLlSlSs130_provenance
{
dgn-np:NP581504.RASkwNmEeEbqA2qLtanETbzkD9vOjpIaE87dnZVLlSlSs130_assertion
dcterms:description
"[In addition, whereas most of the carcinomas showed allelic loss for all three of the probes, indicating a large-scale deletion, several of the carcinomas exhibited losses for only one or two of the probes, thus making it possible, along with the cytogenetic data, to define the least common region of deletion to 3p13----p14.2.]. 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:1686726
;
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:NP581504.RASkwNmEeEbqA2qLtanETbzkD9vOjpIaE87dnZVLlSlSs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:50+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" .
}