@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP510084.RABhvkXAwEcCDAVrHgmqTwVxGKRSLluQJo0EVT98tKsYM
> .
@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:NP510084.RABhvkXAwEcCDAVrHgmqTwVxGKRSLluQJo0EVT98tKsYM130_head
{
this:
np:hasAssertion
dgn-np:NP510084.RABhvkXAwEcCDAVrHgmqTwVxGKRSLluQJo0EVT98tKsYM130_assertion
;
np:hasProvenance
dgn-np:NP510084.RABhvkXAwEcCDAVrHgmqTwVxGKRSLluQJo0EVT98tKsYM130_provenance
;
np:hasPublicationInfo
dgn-np:NP510084.RABhvkXAwEcCDAVrHgmqTwVxGKRSLluQJo0EVT98tKsYM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP510084.RABhvkXAwEcCDAVrHgmqTwVxGKRSLluQJo0EVT98tKsYM130_assertion
a
np:Assertion
.
dgn-np:NP510084.RABhvkXAwEcCDAVrHgmqTwVxGKRSLluQJo0EVT98tKsYM130_provenance
a
np:Provenance
.
dgn-np:NP510084.RABhvkXAwEcCDAVrHgmqTwVxGKRSLluQJo0EVT98tKsYM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP510084.RABhvkXAwEcCDAVrHgmqTwVxGKRSLluQJo0EVT98tKsYM130_assertion
{
miriam-gene:23261
a
ncit:C16612
.
lld:C0206732
a
ncit:C7057
.
dgn-gda:DGN9c0b3ba9f9dcd7eb84ea30437d8b0a2c
sio:SIO_000628
miriam-gene:23261
,
lld:C0206732
;
a
sio:SIO_001121
.
}
dgn-np:NP510084.RABhvkXAwEcCDAVrHgmqTwVxGKRSLluQJo0EVT98tKsYM130_provenance
{
dgn-np:NP510084.RABhvkXAwEcCDAVrHgmqTwVxGKRSLluQJo0EVT98tKsYM130_assertion
dcterms:description
"[Thus, we undertook a molecular analysis of six samples from two patients with multicentric hepatic EHE to test our hypothesis that the presence of identical breakpoints in WWTR1 and CAMTA1 support the monoclonal nature of multifocal EHE.]. 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:22429593
;
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 .
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dgn-np:NP510084.RABhvkXAwEcCDAVrHgmqTwVxGKRSLluQJo0EVT98tKsYM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:04+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
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"v2.1.0" .
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