@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP779110.RASVNkrcYomDrPoKX9BMXEYvbI7YveX7_yL1lLteeOG4g
> .
@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:NP779110.RASVNkrcYomDrPoKX9BMXEYvbI7YveX7_yL1lLteeOG4g130_head
{
this:
np:hasAssertion
dgn-np:NP779110.RASVNkrcYomDrPoKX9BMXEYvbI7YveX7_yL1lLteeOG4g130_assertion
;
np:hasProvenance
dgn-np:NP779110.RASVNkrcYomDrPoKX9BMXEYvbI7YveX7_yL1lLteeOG4g130_provenance
;
np:hasPublicationInfo
dgn-np:NP779110.RASVNkrcYomDrPoKX9BMXEYvbI7YveX7_yL1lLteeOG4g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP779110.RASVNkrcYomDrPoKX9BMXEYvbI7YveX7_yL1lLteeOG4g130_assertion
a
np:Assertion
.
dgn-np:NP779110.RASVNkrcYomDrPoKX9BMXEYvbI7YveX7_yL1lLteeOG4g130_provenance
a
np:Provenance
.
dgn-np:NP779110.RASVNkrcYomDrPoKX9BMXEYvbI7YveX7_yL1lLteeOG4g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP779110.RASVNkrcYomDrPoKX9BMXEYvbI7YveX7_yL1lLteeOG4g130_assertion
{
miriam-gene:6441
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNc8ed2633a643b49de1201ea27d5df40b
sio:SIO_000628
miriam-gene:6441
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP779110.RASVNkrcYomDrPoKX9BMXEYvbI7YveX7_yL1lLteeOG4g130_provenance
{
dgn-np:NP779110.RASVNkrcYomDrPoKX9BMXEYvbI7YveX7_yL1lLteeOG4g130_assertion
dcterms:description
"[Four CpG sites, SP-A1_370, SP-A1_1080, SP-D_1170, and SP-D_1370, were hypomethylated in cancer and were significantly associated with both adenocarcinoma and squamous cell carcinoma, indicating that they have the potential to be used as biomarkers for lung cancer diagnosis and treatment.]. 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:17549420
;
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:NP779110.RASVNkrcYomDrPoKX9BMXEYvbI7YveX7_yL1lLteeOG4g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:52+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" .
}