@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP348199.RAT2oIFZPujWN4XUK2i1v6lX_PxVq2p3ThrJ2B0-8s7JM
> .
@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:NP348199.RAT2oIFZPujWN4XUK2i1v6lX_PxVq2p3ThrJ2B0-8s7JM130_head
{
this:
np:hasAssertion
dgn-np:NP348199.RAT2oIFZPujWN4XUK2i1v6lX_PxVq2p3ThrJ2B0-8s7JM130_assertion
;
np:hasProvenance
dgn-np:NP348199.RAT2oIFZPujWN4XUK2i1v6lX_PxVq2p3ThrJ2B0-8s7JM130_provenance
;
np:hasPublicationInfo
dgn-np:NP348199.RAT2oIFZPujWN4XUK2i1v6lX_PxVq2p3ThrJ2B0-8s7JM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP348199.RAT2oIFZPujWN4XUK2i1v6lX_PxVq2p3ThrJ2B0-8s7JM130_assertion
a
np:Assertion
.
dgn-np:NP348199.RAT2oIFZPujWN4XUK2i1v6lX_PxVq2p3ThrJ2B0-8s7JM130_provenance
a
np:Provenance
.
dgn-np:NP348199.RAT2oIFZPujWN4XUK2i1v6lX_PxVq2p3ThrJ2B0-8s7JM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP348199.RAT2oIFZPujWN4XUK2i1v6lX_PxVq2p3ThrJ2B0-8s7JM130_assertion
{
miriam-gene:10383
a
ncit:C16612
.
lld:C0085541
a
ncit:C7057
.
dgn-gda:DGN14be11f30ca90e0d4ed582f5b35a0124
sio:SIO_000628
miriam-gene:10383
,
lld:C0085541
;
a
sio:SIO_001121
.
}
dgn-np:NP348199.RAT2oIFZPujWN4XUK2i1v6lX_PxVq2p3ThrJ2B0-8s7JM130_provenance
{
dgn-np:NP348199.RAT2oIFZPujWN4XUK2i1v6lX_PxVq2p3ThrJ2B0-8s7JM130_assertion
dcterms:description
"[Furthermore, we believe that, even in those cases where mutations of the alpha4 or the beta2 subunit of the nAChR cosegregate with ADNFLE, there must be some crucial additional factors contributing to the development of the specific symptoms of ADNFLE.]. 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:11512019
;
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:NP348199.RAT2oIFZPujWN4XUK2i1v6lX_PxVq2p3ThrJ2B0-8s7JM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:24+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" .
}