@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP270311.RAc36CwHrxM7moNnuHd4VXvcgORYM497tH14_NLdx7590
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
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http://www.w3.org/2001/XMLSchema#
> .
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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#
> .
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{
this:
np:hasAssertion
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dgn-np:NP270311.RAc36CwHrxM7moNnuHd4VXvcgORYM497tH14_NLdx7590130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP270311.RAc36CwHrxM7moNnuHd4VXvcgORYM497tH14_NLdx7590130_assertion
a
np:Assertion
.
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a
np:Provenance
.
dgn-np:NP270311.RAc36CwHrxM7moNnuHd4VXvcgORYM497tH14_NLdx7590130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP270311.RAc36CwHrxM7moNnuHd4VXvcgORYM497tH14_NLdx7590130_assertion
{
miriam-gene:710
a
ncit:C16612
.
lld:C0019243
a
ncit:C7057
.
dgn-gda:DGN2ae010c1adb588424603ad05ea37cb58
sio:SIO_000628
miriam-gene:710
,
lld:C0019243
;
a
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.
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dgn-np:NP270311.RAc36CwHrxM7moNnuHd4VXvcgORYM497tH14_NLdx7590130_provenance
{
dgn-np:NP270311.RAc36CwHrxM7moNnuHd4VXvcgORYM497tH14_NLdx7590130_assertion
dcterms:description
"[This study constitutes the first molecular analysis of hereditary angioedema (HAE) in Greece, where 11 patients from three unrelated families with recurrent angioedema attacks and decreased C1 inhibitor antigenic levels were analyzed for SERPING1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:19706314
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
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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
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dgn-np:NP270311.RAc36CwHrxM7moNnuHd4VXvcgORYM497tH14_NLdx7590130_publicationInfo
{
this:
dcterms:created
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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
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<
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> , <
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> , <
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> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
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