@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP357490.RA7vZVK9gFhBczBf9QvpNIZH6zTmY9_htsgLNsRaZx4-Q
> .
@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:NP357490.RA7vZVK9gFhBczBf9QvpNIZH6zTmY9_htsgLNsRaZx4-Q130_head
{
this:
np:hasAssertion
dgn-np:NP357490.RA7vZVK9gFhBczBf9QvpNIZH6zTmY9_htsgLNsRaZx4-Q130_assertion
;
np:hasProvenance
dgn-np:NP357490.RA7vZVK9gFhBczBf9QvpNIZH6zTmY9_htsgLNsRaZx4-Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP357490.RA7vZVK9gFhBczBf9QvpNIZH6zTmY9_htsgLNsRaZx4-Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP357490.RA7vZVK9gFhBczBf9QvpNIZH6zTmY9_htsgLNsRaZx4-Q130_assertion
a
np:Assertion
.
dgn-np:NP357490.RA7vZVK9gFhBczBf9QvpNIZH6zTmY9_htsgLNsRaZx4-Q130_provenance
a
np:Provenance
.
dgn-np:NP357490.RA7vZVK9gFhBczBf9QvpNIZH6zTmY9_htsgLNsRaZx4-Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP357490.RA7vZVK9gFhBczBf9QvpNIZH6zTmY9_htsgLNsRaZx4-Q130_assertion
{
miriam-gene:2067
a
ncit:C16612
.
lld:C0242379
a
ncit:C7057
.
dgn-gda:DGNe61114a58d58aae3945cef6b3c6ff36f
sio:SIO_000628
miriam-gene:2067
,
lld:C0242379
;
a
sio:SIO_001121
.
}
dgn-np:NP357490.RA7vZVK9gFhBczBf9QvpNIZH6zTmY9_htsgLNsRaZx4-Q130_provenance
{
dgn-np:NP357490.RA7vZVK9gFhBczBf9QvpNIZH6zTmY9_htsgLNsRaZx4-Q130_assertion
dcterms:description
"[In order to comprehensively capture common genetic variation in the ERCC1 gene, Caucasian data from the International HapMap project was used to assess linkage disequilibrium and choose four tagSNPs (rs1319052, rs3212955, rs3212948, and rs735482) in the ERCC1 gene to genotype 452 lung cancer cases, 175 H&N cancer cases, and 790 healthy controls.]. 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:20863778
;
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:NP357490.RA7vZVK9gFhBczBf9QvpNIZH6zTmY9_htsgLNsRaZx4-Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:29+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" .
}