@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP82208.RAB0wACXo9532Vl7bg91pwDfTwkWkz7eGmmut4QYv5kR4
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP82208.RAB0wACXo9532Vl7bg91pwDfTwkWkz7eGmmut4QYv5kR4130_head
{
this:
np:hasAssertion
dgn-np:NP82208.RAB0wACXo9532Vl7bg91pwDfTwkWkz7eGmmut4QYv5kR4130_assertion
;
np:hasProvenance
dgn-np:NP82208.RAB0wACXo9532Vl7bg91pwDfTwkWkz7eGmmut4QYv5kR4130_provenance
;
np:hasPublicationInfo
dgn-np:NP82208.RAB0wACXo9532Vl7bg91pwDfTwkWkz7eGmmut4QYv5kR4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP82208.RAB0wACXo9532Vl7bg91pwDfTwkWkz7eGmmut4QYv5kR4130_assertion
a
np:Assertion
.
dgn-np:NP82208.RAB0wACXo9532Vl7bg91pwDfTwkWkz7eGmmut4QYv5kR4130_provenance
a
np:Provenance
.
dgn-np:NP82208.RAB0wACXo9532Vl7bg91pwDfTwkWkz7eGmmut4QYv5kR4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP82208.RAB0wACXo9532Vl7bg91pwDfTwkWkz7eGmmut4QYv5kR4130_assertion
{
miriam-gene:4292
a
ncit:C16612
.
lld:C0346647
a
ncit:C7057
.
dgn-gda:DGN32880ceb1d04e193b28e9df38cdffae4
sio:SIO_000628
miriam-gene:4292
,
lld:C0346647
;
a
sio:SIO_001122
.
}
dgn-np:NP82208.RAB0wACXo9532Vl7bg91pwDfTwkWkz7eGmmut4QYv5kR4130_provenance
{
dgn-np:NP82208.RAB0wACXo9532Vl7bg91pwDfTwkWkz7eGmmut4QYv5kR4130_assertion
dcterms:description
"[This study supports the premise that the occurrence of rare (especially double primary) cancers does indicate an increased cancer susceptibility, although the numbers of cases ascertained were too small to draw firm conclusions.]. 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:14574163
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP82208.RAB0wACXo9532Vl7bg91pwDfTwkWkz7eGmmut4QYv5kR4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:25+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}