@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP350222.RAzE4ORkDD7HKMHA7B3zgsFV33M_CR0U09sU7pVgwBIzk
> .
@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:NP350222.RAzE4ORkDD7HKMHA7B3zgsFV33M_CR0U09sU7pVgwBIzk130_head
{
this:
np:hasAssertion
dgn-np:NP350222.RAzE4ORkDD7HKMHA7B3zgsFV33M_CR0U09sU7pVgwBIzk130_assertion
;
np:hasProvenance
dgn-np:NP350222.RAzE4ORkDD7HKMHA7B3zgsFV33M_CR0U09sU7pVgwBIzk130_provenance
;
np:hasPublicationInfo
dgn-np:NP350222.RAzE4ORkDD7HKMHA7B3zgsFV33M_CR0U09sU7pVgwBIzk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP350222.RAzE4ORkDD7HKMHA7B3zgsFV33M_CR0U09sU7pVgwBIzk130_assertion
a
np:Assertion
.
dgn-np:NP350222.RAzE4ORkDD7HKMHA7B3zgsFV33M_CR0U09sU7pVgwBIzk130_provenance
a
np:Provenance
.
dgn-np:NP350222.RAzE4ORkDD7HKMHA7B3zgsFV33M_CR0U09sU7pVgwBIzk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP350222.RAzE4ORkDD7HKMHA7B3zgsFV33M_CR0U09sU7pVgwBIzk130_assertion
{
miriam-gene:328
a
ncit:C16612
.
lld:C0684249
a
ncit:C7057
.
dgn-gda:DGNa74302dc86fc21805873d876b67f2ca0
sio:SIO_000628
miriam-gene:328
,
lld:C0684249
;
a
sio:SIO_001121
.
}
dgn-np:NP350222.RAzE4ORkDD7HKMHA7B3zgsFV33M_CR0U09sU7pVgwBIzk130_provenance
{
dgn-np:NP350222.RAzE4ORkDD7HKMHA7B3zgsFV33M_CR0U09sU7pVgwBIzk130_assertion
dcterms:description
"[Our results suggest that polymorphism Asn118Asn in ERCC1, A67T in iASPP and Asn148Glu in APE1 may associated with early onset of lung cancer as well as some specific subtype 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:20354815
;
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:NP350222.RAzE4ORkDD7HKMHA7B3zgsFV33M_CR0U09sU7pVgwBIzk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:25+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" .
}