@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP355593.RAc4EDChuqri7wAo1x3nMM6n0QcvZyQgSJbu4IOMZaNx4
> .
@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:NP355593.RAc4EDChuqri7wAo1x3nMM6n0QcvZyQgSJbu4IOMZaNx4130_head
{
this:
np:hasAssertion
dgn-np:NP355593.RAc4EDChuqri7wAo1x3nMM6n0QcvZyQgSJbu4IOMZaNx4130_assertion
;
np:hasProvenance
dgn-np:NP355593.RAc4EDChuqri7wAo1x3nMM6n0QcvZyQgSJbu4IOMZaNx4130_provenance
;
np:hasPublicationInfo
dgn-np:NP355593.RAc4EDChuqri7wAo1x3nMM6n0QcvZyQgSJbu4IOMZaNx4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP355593.RAc4EDChuqri7wAo1x3nMM6n0QcvZyQgSJbu4IOMZaNx4130_assertion
a
np:Assertion
.
dgn-np:NP355593.RAc4EDChuqri7wAo1x3nMM6n0QcvZyQgSJbu4IOMZaNx4130_provenance
a
np:Provenance
.
dgn-np:NP355593.RAc4EDChuqri7wAo1x3nMM6n0QcvZyQgSJbu4IOMZaNx4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP355593.RAc4EDChuqri7wAo1x3nMM6n0QcvZyQgSJbu4IOMZaNx4130_assertion
{
miriam-gene:196883
a
ncit:C16612
.
lld:C0149925
a
ncit:C7057
.
dgn-gda:DGN7f03f9a83a80bbe8628dc80203f39237
sio:SIO_000628
miriam-gene:196883
,
lld:C0149925
;
a
sio:SIO_001121
.
}
dgn-np:NP355593.RAc4EDChuqri7wAo1x3nMM6n0QcvZyQgSJbu4IOMZaNx4130_provenance
{
dgn-np:NP355593.RAc4EDChuqri7wAo1x3nMM6n0QcvZyQgSJbu4IOMZaNx4130_assertion
dcterms:description
"[DNA underrepresentations of 11q were the most frequent findings in TC (8 of 17) and AC (4 of 6), whereas these aberrations were rare in LCNEC (1 of 3) and SCLC (0 of 3).]. 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:9777940
;
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:NP355593.RAc4EDChuqri7wAo1x3nMM6n0QcvZyQgSJbu4IOMZaNx4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:28+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" .
}