@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP222687.RApyLBXCR-aHVXbGo3Ra2HByagfGUkjK-zhYEcJAJMyrU
> .
@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:NP222687.RApyLBXCR-aHVXbGo3Ra2HByagfGUkjK-zhYEcJAJMyrU130_head
{
this:
np:hasAssertion
dgn-np:NP222687.RApyLBXCR-aHVXbGo3Ra2HByagfGUkjK-zhYEcJAJMyrU130_assertion
;
np:hasProvenance
dgn-np:NP222687.RApyLBXCR-aHVXbGo3Ra2HByagfGUkjK-zhYEcJAJMyrU130_provenance
;
np:hasPublicationInfo
dgn-np:NP222687.RApyLBXCR-aHVXbGo3Ra2HByagfGUkjK-zhYEcJAJMyrU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP222687.RApyLBXCR-aHVXbGo3Ra2HByagfGUkjK-zhYEcJAJMyrU130_assertion
a
np:Assertion
.
dgn-np:NP222687.RApyLBXCR-aHVXbGo3Ra2HByagfGUkjK-zhYEcJAJMyrU130_provenance
a
np:Provenance
.
dgn-np:NP222687.RApyLBXCR-aHVXbGo3Ra2HByagfGUkjK-zhYEcJAJMyrU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP222687.RApyLBXCR-aHVXbGo3Ra2HByagfGUkjK-zhYEcJAJMyrU130_assertion
{
miriam-gene:3141
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN424d163864ab104121c4d22143c3aeac
sio:SIO_000628
miriam-gene:3141
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP222687.RApyLBXCR-aHVXbGo3Ra2HByagfGUkjK-zhYEcJAJMyrU130_provenance
{
dgn-np:NP222687.RApyLBXCR-aHVXbGo3Ra2HByagfGUkjK-zhYEcJAJMyrU130_assertion
dcterms:description
"[HCS, which accounts for approximately 5%-10% of all malignancies, is characterized by diagnosis of the same malignancy in multiple family members, an earlier age of onset than expected, an increased frequency of bilateral cancers in paired organs, and the presence of premalignant syndromes.]. 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:7675683
;
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:NP222687.RApyLBXCR-aHVXbGo3Ra2HByagfGUkjK-zhYEcJAJMyrU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:03+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" .
}