@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP812563.RA7sqEwEukav_q6b5EXHZksWzCKbu8vUc-pMNh2Mp5KbA
> .
@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:NP812563.RA7sqEwEukav_q6b5EXHZksWzCKbu8vUc-pMNh2Mp5KbA130_head
{
this:
np:hasAssertion
dgn-np:NP812563.RA7sqEwEukav_q6b5EXHZksWzCKbu8vUc-pMNh2Mp5KbA130_assertion
;
np:hasProvenance
dgn-np:NP812563.RA7sqEwEukav_q6b5EXHZksWzCKbu8vUc-pMNh2Mp5KbA130_provenance
;
np:hasPublicationInfo
dgn-np:NP812563.RA7sqEwEukav_q6b5EXHZksWzCKbu8vUc-pMNh2Mp5KbA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP812563.RA7sqEwEukav_q6b5EXHZksWzCKbu8vUc-pMNh2Mp5KbA130_assertion
a
np:Assertion
.
dgn-np:NP812563.RA7sqEwEukav_q6b5EXHZksWzCKbu8vUc-pMNh2Mp5KbA130_provenance
a
np:Provenance
.
dgn-np:NP812563.RA7sqEwEukav_q6b5EXHZksWzCKbu8vUc-pMNh2Mp5KbA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP812563.RA7sqEwEukav_q6b5EXHZksWzCKbu8vUc-pMNh2Mp5KbA130_assertion
{
miriam-gene:462
a
ncit:C16612
.
lld:C0019243
a
ncit:C7057
.
dgn-gda:DGNca8b91d53bcb889d932a40a64cc1f1f0
sio:SIO_000628
miriam-gene:462
,
lld:C0019243
;
a
sio:SIO_001121
.
}
dgn-np:NP812563.RA7sqEwEukav_q6b5EXHZksWzCKbu8vUc-pMNh2Mp5KbA130_provenance
{
dgn-np:NP812563.RA7sqEwEukav_q6b5EXHZksWzCKbu8vUc-pMNh2Mp5KbA130_assertion
dcterms:description
"[Hereditary angioedema (HAE), characterized by recurrent episodes of angioedema involving the skin, or the mucosa of the upper respiratory or the gastrointestinal tracts, results from heterozygosity for deficiency of the serine proteinase inhibitor (serpin), C1 inhibitor (C1INH).]. 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:15596403
;
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:NP812563.RA7sqEwEukav_q6b5EXHZksWzCKbu8vUc-pMNh2Mp5KbA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:18+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" .
}