@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP647710.RAkIpaRgzV2OPergIq0NZ1Qe1WWvr3Dw896pdiqkEUs2s
> .
@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:NP647710.RAkIpaRgzV2OPergIq0NZ1Qe1WWvr3Dw896pdiqkEUs2s130_head
{
this:
np:hasAssertion
dgn-np:NP647710.RAkIpaRgzV2OPergIq0NZ1Qe1WWvr3Dw896pdiqkEUs2s130_assertion
;
np:hasProvenance
dgn-np:NP647710.RAkIpaRgzV2OPergIq0NZ1Qe1WWvr3Dw896pdiqkEUs2s130_provenance
;
np:hasPublicationInfo
dgn-np:NP647710.RAkIpaRgzV2OPergIq0NZ1Qe1WWvr3Dw896pdiqkEUs2s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP647710.RAkIpaRgzV2OPergIq0NZ1Qe1WWvr3Dw896pdiqkEUs2s130_assertion
a
np:Assertion
.
dgn-np:NP647710.RAkIpaRgzV2OPergIq0NZ1Qe1WWvr3Dw896pdiqkEUs2s130_provenance
a
np:Provenance
.
dgn-np:NP647710.RAkIpaRgzV2OPergIq0NZ1Qe1WWvr3Dw896pdiqkEUs2s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP647710.RAkIpaRgzV2OPergIq0NZ1Qe1WWvr3Dw896pdiqkEUs2s130_assertion
{
miriam-gene:54205
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN632b10f23fb6d3e2c9849b6c2e7d5bee
sio:SIO_000628
miriam-gene:54205
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP647710.RAkIpaRgzV2OPergIq0NZ1Qe1WWvr3Dw896pdiqkEUs2s130_provenance
{
dgn-np:NP647710.RAkIpaRgzV2OPergIq0NZ1Qe1WWvr3Dw896pdiqkEUs2s130_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:NP647710.RAkIpaRgzV2OPergIq0NZ1Qe1WWvr3Dw896pdiqkEUs2s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:30+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" .
}