@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP892355.RAgnuCZpC591XAP9xZEj0LUnvAP4efouMmci6115exnos
> .
@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:NP892355.RAgnuCZpC591XAP9xZEj0LUnvAP4efouMmci6115exnos130_head
{
this:
np:hasAssertion
dgn-np:NP892355.RAgnuCZpC591XAP9xZEj0LUnvAP4efouMmci6115exnos130_assertion
;
np:hasProvenance
dgn-np:NP892355.RAgnuCZpC591XAP9xZEj0LUnvAP4efouMmci6115exnos130_provenance
;
np:hasPublicationInfo
dgn-np:NP892355.RAgnuCZpC591XAP9xZEj0LUnvAP4efouMmci6115exnos130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP892355.RAgnuCZpC591XAP9xZEj0LUnvAP4efouMmci6115exnos130_assertion
a
np:Assertion
.
dgn-np:NP892355.RAgnuCZpC591XAP9xZEj0LUnvAP4efouMmci6115exnos130_provenance
a
np:Provenance
.
dgn-np:NP892355.RAgnuCZpC591XAP9xZEj0LUnvAP4efouMmci6115exnos130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP892355.RAgnuCZpC591XAP9xZEj0LUnvAP4efouMmci6115exnos130_assertion
{
miriam-gene:3251
a
ncit:C16612
.
lld:C0278704
a
ncit:C7057
.
dgn-gda:DGNeb9b3beb0845358471cf64f50d15861f
sio:SIO_000628
miriam-gene:3251
,
lld:C0278704
;
a
sio:SIO_001121
.
}
dgn-np:NP892355.RAgnuCZpC591XAP9xZEj0LUnvAP4efouMmci6115exnos130_provenance
{
dgn-np:NP892355.RAgnuCZpC591XAP9xZEj0LUnvAP4efouMmci6115exnos130_assertion
dcterms:description
"[Specific patterns of HPRT mutations are utilized to distinguish these various potential sources of carcinogenic exposures in the drinking water of families with childhood cancer and to differentiate chemically or radiologically induced cancers from those which occur spontaneously.]. 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:11130945
;
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:NP892355.RAgnuCZpC591XAP9xZEj0LUnvAP4efouMmci6115exnos130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:08+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" .
}