@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP318448.RAEfVU78eEOE3IW8-SKK5wmM26hxP2Y_uUG4aWhMBQNoE
> .
@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:NP318448.RAEfVU78eEOE3IW8-SKK5wmM26hxP2Y_uUG4aWhMBQNoE130_head
{
this:
np:hasAssertion
dgn-np:NP318448.RAEfVU78eEOE3IW8-SKK5wmM26hxP2Y_uUG4aWhMBQNoE130_assertion
;
np:hasProvenance
dgn-np:NP318448.RAEfVU78eEOE3IW8-SKK5wmM26hxP2Y_uUG4aWhMBQNoE130_provenance
;
np:hasPublicationInfo
dgn-np:NP318448.RAEfVU78eEOE3IW8-SKK5wmM26hxP2Y_uUG4aWhMBQNoE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP318448.RAEfVU78eEOE3IW8-SKK5wmM26hxP2Y_uUG4aWhMBQNoE130_assertion
a
np:Assertion
.
dgn-np:NP318448.RAEfVU78eEOE3IW8-SKK5wmM26hxP2Y_uUG4aWhMBQNoE130_provenance
a
np:Provenance
.
dgn-np:NP318448.RAEfVU78eEOE3IW8-SKK5wmM26hxP2Y_uUG4aWhMBQNoE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP318448.RAEfVU78eEOE3IW8-SKK5wmM26hxP2Y_uUG4aWhMBQNoE130_assertion
{
miriam-gene:3265
a
ncit:C16612
.
lld:C0242379
a
ncit:C7057
.
dgn-gda:DGN9b8173b6e83c048d6653cb6e8c7ce075
sio:SIO_000628
miriam-gene:3265
,
lld:C0242379
;
a
sio:SIO_001121
.
}
dgn-np:NP318448.RAEfVU78eEOE3IW8-SKK5wmM26hxP2Y_uUG4aWhMBQNoE130_provenance
{
dgn-np:NP318448.RAEfVU78eEOE3IW8-SKK5wmM26hxP2Y_uUG4aWhMBQNoE130_assertion
dcterms:description
"[The smallest common regions of allele loss were located between D11S1758 and D11S12 in the centromeric region of chromosome segment 11p15.5 (region of LOH on chromosome 11 in lung cancer, LOH11A) and between HRAS and D11S1363 in the telomeric region (region of LOH on chromosome 11 in lung cancer, LOH11B).]. 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:9115960
;
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:NP318448.RAEfVU78eEOE3IW8-SKK5wmM26hxP2Y_uUG4aWhMBQNoE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:04+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" .
}