@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP262535.RADdQRGMVdxQjUFrpEKo0mywLMUhwqvUnb9_ApOzVULak
> .
@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:NP262535.RADdQRGMVdxQjUFrpEKo0mywLMUhwqvUnb9_ApOzVULak130_head
{
this:
np:hasAssertion
dgn-np:NP262535.RADdQRGMVdxQjUFrpEKo0mywLMUhwqvUnb9_ApOzVULak130_assertion
;
np:hasProvenance
dgn-np:NP262535.RADdQRGMVdxQjUFrpEKo0mywLMUhwqvUnb9_ApOzVULak130_provenance
;
np:hasPublicationInfo
dgn-np:NP262535.RADdQRGMVdxQjUFrpEKo0mywLMUhwqvUnb9_ApOzVULak130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP262535.RADdQRGMVdxQjUFrpEKo0mywLMUhwqvUnb9_ApOzVULak130_assertion
a
np:Assertion
.
dgn-np:NP262535.RADdQRGMVdxQjUFrpEKo0mywLMUhwqvUnb9_ApOzVULak130_provenance
a
np:Provenance
.
dgn-np:NP262535.RADdQRGMVdxQjUFrpEKo0mywLMUhwqvUnb9_ApOzVULak130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP262535.RADdQRGMVdxQjUFrpEKo0mywLMUhwqvUnb9_ApOzVULak130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0684249
a
ncit:C7057
.
dgn-gda:DGN4f3e89545d0c8af659ab745bbcdf7c2f
sio:SIO_000628
miriam-gene:1029
,
lld:C0684249
;
a
sio:SIO_001121
.
}
dgn-np:NP262535.RADdQRGMVdxQjUFrpEKo0mywLMUhwqvUnb9_ApOzVULak130_provenance
{
dgn-np:NP262535.RADdQRGMVdxQjUFrpEKo0mywLMUhwqvUnb9_ApOzVULak130_assertion
dcterms:description
"[In conclusion, the frequency of p16INK4A or CDH13 hypermethylation in patient serum, together with evidence of their early occurrence in lung cancerogenesis and the total lack of methylation in serum from healthy individuals, offer a promising tool for non invasive early detection of lung cancer.]. 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:16222700
;
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:NP262535.RADdQRGMVdxQjUFrpEKo0mywLMUhwqvUnb9_ApOzVULak130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:26+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" .
}