@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP489877.RASpHADzLsnum6NJTWbmfqWkO8clGjqoJ7s95ODvdfn3s
> .
@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:NP489877.RASpHADzLsnum6NJTWbmfqWkO8clGjqoJ7s95ODvdfn3s130_head
{
this:
np:hasAssertion
dgn-np:NP489877.RASpHADzLsnum6NJTWbmfqWkO8clGjqoJ7s95ODvdfn3s130_assertion
;
np:hasProvenance
dgn-np:NP489877.RASpHADzLsnum6NJTWbmfqWkO8clGjqoJ7s95ODvdfn3s130_provenance
;
np:hasPublicationInfo
dgn-np:NP489877.RASpHADzLsnum6NJTWbmfqWkO8clGjqoJ7s95ODvdfn3s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP489877.RASpHADzLsnum6NJTWbmfqWkO8clGjqoJ7s95ODvdfn3s130_assertion
a
np:Assertion
.
dgn-np:NP489877.RASpHADzLsnum6NJTWbmfqWkO8clGjqoJ7s95ODvdfn3s130_provenance
a
np:Provenance
.
dgn-np:NP489877.RASpHADzLsnum6NJTWbmfqWkO8clGjqoJ7s95ODvdfn3s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP489877.RASpHADzLsnum6NJTWbmfqWkO8clGjqoJ7s95ODvdfn3s130_assertion
{
miriam-gene:1791
a
ncit:C16612
.
lld:C0007847
a
ncit:C7057
.
dgn-gda:DGN291843028ebcf3f059b5ad5eef601cfe
sio:SIO_000628
miriam-gene:1791
,
lld:C0007847
;
a
sio:SIO_001121
.
}
dgn-np:NP489877.RASpHADzLsnum6NJTWbmfqWkO8clGjqoJ7s95ODvdfn3s130_provenance
{
dgn-np:NP489877.RASpHADzLsnum6NJTWbmfqWkO8clGjqoJ7s95ODvdfn3s130_assertion
dcterms:description
"[Based on single SNP TDT tests we identified 16 significant SNPs in the discover stage and six of 14 SNPs that could be assayed by TaqMan were significantly overtransmitted in women with cervical cancer in the combined replication set.]. 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:23927961
;
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:NP489877.RASpHADzLsnum6NJTWbmfqWkO8clGjqoJ7s95ODvdfn3s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:52+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" .
}