@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP792153.RANjy1L6Uk7OipGQxPLXsB1PowQ7Gar_cKAIi7omaFE9s
> .
@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:NP792153.RANjy1L6Uk7OipGQxPLXsB1PowQ7Gar_cKAIi7omaFE9s130_head
{
this:
np:hasAssertion
dgn-np:NP792153.RANjy1L6Uk7OipGQxPLXsB1PowQ7Gar_cKAIi7omaFE9s130_assertion
;
np:hasProvenance
dgn-np:NP792153.RANjy1L6Uk7OipGQxPLXsB1PowQ7Gar_cKAIi7omaFE9s130_provenance
;
np:hasPublicationInfo
dgn-np:NP792153.RANjy1L6Uk7OipGQxPLXsB1PowQ7Gar_cKAIi7omaFE9s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP792153.RANjy1L6Uk7OipGQxPLXsB1PowQ7Gar_cKAIi7omaFE9s130_assertion
a
np:Assertion
.
dgn-np:NP792153.RANjy1L6Uk7OipGQxPLXsB1PowQ7Gar_cKAIi7omaFE9s130_provenance
a
np:Provenance
.
dgn-np:NP792153.RANjy1L6Uk7OipGQxPLXsB1PowQ7Gar_cKAIi7omaFE9s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP792153.RANjy1L6Uk7OipGQxPLXsB1PowQ7Gar_cKAIi7omaFE9s130_assertion
{
miriam-gene:2030
a
ncit:C16612
.
lld:C0007131
a
ncit:C7057
.
dgn-gda:DGN3dde6240b4cddef7586915e2811b48c3
sio:SIO_000628
miriam-gene:2030
,
lld:C0007131
;
a
sio:SIO_001121
.
}
dgn-np:NP792153.RANjy1L6Uk7OipGQxPLXsB1PowQ7Gar_cKAIi7omaFE9s130_provenance
{
dgn-np:NP792153.RANjy1L6Uk7OipGQxPLXsB1PowQ7Gar_cKAIi7omaFE9s130_assertion
dcterms:description
"[Five SNPs in four genes (CDA, NT5C2, RRM1, and SLC29A1) showed associations with OS of those patients with NSCLC, as well as nine haplotypes in four genes (RRM1, RRM2, SLC28A3, and SLC29A1) with a P value of less than 0.05.]. 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:22173087
;
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:NP792153.RANjy1L6Uk7OipGQxPLXsB1PowQ7Gar_cKAIi7omaFE9s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:06+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" .
}