@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP883015.RAHwtKTnXo8CIFSRNvtk1tSPlR9BtM-NRMW32fSUDAONY
> .
@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:NP883015.RAHwtKTnXo8CIFSRNvtk1tSPlR9BtM-NRMW32fSUDAONY130_head
{
this:
np:hasAssertion
dgn-np:NP883015.RAHwtKTnXo8CIFSRNvtk1tSPlR9BtM-NRMW32fSUDAONY130_assertion
;
np:hasProvenance
dgn-np:NP883015.RAHwtKTnXo8CIFSRNvtk1tSPlR9BtM-NRMW32fSUDAONY130_provenance
;
np:hasPublicationInfo
dgn-np:NP883015.RAHwtKTnXo8CIFSRNvtk1tSPlR9BtM-NRMW32fSUDAONY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP883015.RAHwtKTnXo8CIFSRNvtk1tSPlR9BtM-NRMW32fSUDAONY130_assertion
a
np:Assertion
.
dgn-np:NP883015.RAHwtKTnXo8CIFSRNvtk1tSPlR9BtM-NRMW32fSUDAONY130_provenance
a
np:Provenance
.
dgn-np:NP883015.RAHwtKTnXo8CIFSRNvtk1tSPlR9BtM-NRMW32fSUDAONY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP883015.RAHwtKTnXo8CIFSRNvtk1tSPlR9BtM-NRMW32fSUDAONY130_assertion
{
miriam-gene:5624
a
ncit:C16612
.
lld:C0007131
a
ncit:C7057
.
dgn-gda:DGN52b8044d96fe2a0bebd3df967ed37c74
sio:SIO_000628
miriam-gene:5624
,
lld:C0007131
;
a
sio:SIO_001121
.
}
dgn-np:NP883015.RAHwtKTnXo8CIFSRNvtk1tSPlR9BtM-NRMW32fSUDAONY130_provenance
{
dgn-np:NP883015.RAHwtKTnXo8CIFSRNvtk1tSPlR9BtM-NRMW32fSUDAONY130_assertion
dcterms:description
"[Allelic loss at 9p21 (p16 locus), 17p13 (p53) and 5q21(APC) has been frequently described in NSCLC and has also been described in premalignant epithelial lesions of the bronchus and normal bronchial cells.]. 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:17330809
;
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:NP883015.RAHwtKTnXo8CIFSRNvtk1tSPlR9BtM-NRMW32fSUDAONY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:59+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" .
}