@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP773296.RA2ZlBPP9Wzx5pk9VdHPY8a498kilfjBO3XTJgPI2mAss
> .
@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:NP773296.RA2ZlBPP9Wzx5pk9VdHPY8a498kilfjBO3XTJgPI2mAss130_head
{
this:
np:hasAssertion
dgn-np:NP773296.RA2ZlBPP9Wzx5pk9VdHPY8a498kilfjBO3XTJgPI2mAss130_assertion
;
np:hasProvenance
dgn-np:NP773296.RA2ZlBPP9Wzx5pk9VdHPY8a498kilfjBO3XTJgPI2mAss130_provenance
;
np:hasPublicationInfo
dgn-np:NP773296.RA2ZlBPP9Wzx5pk9VdHPY8a498kilfjBO3XTJgPI2mAss130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP773296.RA2ZlBPP9Wzx5pk9VdHPY8a498kilfjBO3XTJgPI2mAss130_assertion
a
np:Assertion
.
dgn-np:NP773296.RA2ZlBPP9Wzx5pk9VdHPY8a498kilfjBO3XTJgPI2mAss130_provenance
a
np:Provenance
.
dgn-np:NP773296.RA2ZlBPP9Wzx5pk9VdHPY8a498kilfjBO3XTJgPI2mAss130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP773296.RA2ZlBPP9Wzx5pk9VdHPY8a498kilfjBO3XTJgPI2mAss130_assertion
{
miriam-gene:100380873
a
ncit:C16612
.
lld:C1562113
a
ncit:C7057
.
dgn-gda:DGN92f5dafa96c6be9778710533f60e9f16
sio:SIO_000628
miriam-gene:100380873
,
lld:C1562113
;
a
sio:SIO_001121
.
}
dgn-np:NP773296.RA2ZlBPP9Wzx5pk9VdHPY8a498kilfjBO3XTJgPI2mAss130_provenance
{
dgn-np:NP773296.RA2ZlBPP9Wzx5pk9VdHPY8a498kilfjBO3XTJgPI2mAss130_assertion
dcterms:description
"[The incomplete penetrance and high phenocopy rate observed at FCD2 suggest that the origin of FCD in these three families is complex and also depends on other genetic loci or environmental factors.]. 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:16936105
;
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:NP773296.RA2ZlBPP9Wzx5pk9VdHPY8a498kilfjBO3XTJgPI2mAss130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:47+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" .
}