@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP760793.RAEVrqLUg28Ja1ctVNkI3_cR5Gccv8klp_jmedxkR67wA
> .
@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:NP760793.RAEVrqLUg28Ja1ctVNkI3_cR5Gccv8klp_jmedxkR67wA130_head
{
this:
np:hasAssertion
dgn-np:NP760793.RAEVrqLUg28Ja1ctVNkI3_cR5Gccv8klp_jmedxkR67wA130_assertion
;
np:hasProvenance
dgn-np:NP760793.RAEVrqLUg28Ja1ctVNkI3_cR5Gccv8klp_jmedxkR67wA130_provenance
;
np:hasPublicationInfo
dgn-np:NP760793.RAEVrqLUg28Ja1ctVNkI3_cR5Gccv8klp_jmedxkR67wA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP760793.RAEVrqLUg28Ja1ctVNkI3_cR5Gccv8klp_jmedxkR67wA130_assertion
a
np:Assertion
.
dgn-np:NP760793.RAEVrqLUg28Ja1ctVNkI3_cR5Gccv8klp_jmedxkR67wA130_provenance
a
np:Provenance
.
dgn-np:NP760793.RAEVrqLUg28Ja1ctVNkI3_cR5Gccv8klp_jmedxkR67wA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP760793.RAEVrqLUg28Ja1ctVNkI3_cR5Gccv8klp_jmedxkR67wA130_assertion
{
miriam-gene:196883
a
ncit:C16612
.
lld:C0334299
a
ncit:C7057
.
dgn-gda:DGNa67d889dd56df3de92aec11707b20cf9
sio:SIO_000628
miriam-gene:196883
,
lld:C0334299
;
a
sio:SIO_001121
.
}
dgn-np:NP760793.RAEVrqLUg28Ja1ctVNkI3_cR5Gccv8klp_jmedxkR67wA130_provenance
{
dgn-np:NP760793.RAEVrqLUg28Ja1ctVNkI3_cR5Gccv8klp_jmedxkR67wA130_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:NP760793.RAEVrqLUg28Ja1ctVNkI3_cR5Gccv8klp_jmedxkR67wA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:40+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" .
}