@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP419398.RAWPF62FLX2MYJJEnb4kkaSle6QMB3JC2-F4Hrw4pf8kA
> .
@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:NP419398.RAWPF62FLX2MYJJEnb4kkaSle6QMB3JC2-F4Hrw4pf8kA130_head
{
this:
np:hasAssertion
dgn-np:NP419398.RAWPF62FLX2MYJJEnb4kkaSle6QMB3JC2-F4Hrw4pf8kA130_assertion
;
np:hasProvenance
dgn-np:NP419398.RAWPF62FLX2MYJJEnb4kkaSle6QMB3JC2-F4Hrw4pf8kA130_provenance
;
np:hasPublicationInfo
dgn-np:NP419398.RAWPF62FLX2MYJJEnb4kkaSle6QMB3JC2-F4Hrw4pf8kA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP419398.RAWPF62FLX2MYJJEnb4kkaSle6QMB3JC2-F4Hrw4pf8kA130_assertion
a
np:Assertion
.
dgn-np:NP419398.RAWPF62FLX2MYJJEnb4kkaSle6QMB3JC2-F4Hrw4pf8kA130_provenance
a
np:Provenance
.
dgn-np:NP419398.RAWPF62FLX2MYJJEnb4kkaSle6QMB3JC2-F4Hrw4pf8kA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP419398.RAWPF62FLX2MYJJEnb4kkaSle6QMB3JC2-F4Hrw4pf8kA130_assertion
{
miriam-gene:5071
a
ncit:C16612
.
lld:C0242379
a
ncit:C7057
.
dgn-gda:DGN69ca976bc90bfbbba1fdbc3a54699b29
sio:SIO_000628
miriam-gene:5071
,
lld:C0242379
;
a
sio:SIO_001121
.
}
dgn-np:NP419398.RAWPF62FLX2MYJJEnb4kkaSle6QMB3JC2-F4Hrw4pf8kA130_provenance
{
dgn-np:NP419398.RAWPF62FLX2MYJJEnb4kkaSle6QMB3JC2-F4Hrw4pf8kA130_assertion
dcterms:description
"[In accordance with the developmental mode of lung cancer established by Sekine et al., we assumed that the occurrence and development of lung cancer were linked not only to gene loss in the 3p region (WNT7A, 3p25) and genetic mutations in the 9p region but also to similar events in the regions of 1p36.2 (FRAP1), 6q25.2-q27 (PARK2), and 11q13 (CCND1).]. 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:23237220
;
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:NP419398.RAWPF62FLX2MYJJEnb4kkaSle6QMB3JC2-F4Hrw4pf8kA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:09+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" .
}