@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1104886.RAHYAfwmA06K4N8sb6iuVd7BeA56p9eqpXeoeYgyP-P8U
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1104886.RAHYAfwmA06K4N8sb6iuVd7BeA56p9eqpXeoeYgyP-P8U130_head
{
this:
np:hasAssertion
dgn-np:NP1104886.RAHYAfwmA06K4N8sb6iuVd7BeA56p9eqpXeoeYgyP-P8U130_assertion
;
np:hasProvenance
dgn-np:NP1104886.RAHYAfwmA06K4N8sb6iuVd7BeA56p9eqpXeoeYgyP-P8U130_provenance
;
np:hasPublicationInfo
dgn-np:NP1104886.RAHYAfwmA06K4N8sb6iuVd7BeA56p9eqpXeoeYgyP-P8U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1104886.RAHYAfwmA06K4N8sb6iuVd7BeA56p9eqpXeoeYgyP-P8U130_assertion
a
np:Assertion
.
dgn-np:NP1104886.RAHYAfwmA06K4N8sb6iuVd7BeA56p9eqpXeoeYgyP-P8U130_provenance
a
np:Provenance
.
dgn-np:NP1104886.RAHYAfwmA06K4N8sb6iuVd7BeA56p9eqpXeoeYgyP-P8U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1104886.RAHYAfwmA06K4N8sb6iuVd7BeA56p9eqpXeoeYgyP-P8U130_assertion
{
miriam-gene:4210
a
ncit:C16612
.
lld:C0031069
a
ncit:C7057
.
dgn-gda:DGNc78d1ea54900f7a64393fdca7dc66852
sio:SIO_000628
miriam-gene:4210
,
lld:C0031069
;
a
sio:SIO_001122
.
}
dgn-np:NP1104886.RAHYAfwmA06K4N8sb6iuVd7BeA56p9eqpXeoeYgyP-P8U130_provenance
{
dgn-np:NP1104886.RAHYAfwmA06K4N8sb6iuVd7BeA56p9eqpXeoeYgyP-P8U130_assertion
dcterms:description
"[We screened 207 BD patients who had no symptoms and family history for FMF and 200 healthy subjects for five common MEFV gene mutations (E148Q, M680I, M694V, V726A, P369S) and clinical features.]. 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:23973724
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1104886.RAHYAfwmA06K4N8sb6iuVd7BeA56p9eqpXeoeYgyP-P8U130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:06+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}