@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP666671.RAS01yjRx4TttkvNnlrmqgrvyOqpr-Ge-NRl9WJDYro-A
> .
@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:NP666671.RAS01yjRx4TttkvNnlrmqgrvyOqpr-Ge-NRl9WJDYro-A130_head
{
this:
np:hasAssertion
dgn-np:NP666671.RAS01yjRx4TttkvNnlrmqgrvyOqpr-Ge-NRl9WJDYro-A130_assertion
;
np:hasProvenance
dgn-np:NP666671.RAS01yjRx4TttkvNnlrmqgrvyOqpr-Ge-NRl9WJDYro-A130_provenance
;
np:hasPublicationInfo
dgn-np:NP666671.RAS01yjRx4TttkvNnlrmqgrvyOqpr-Ge-NRl9WJDYro-A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP666671.RAS01yjRx4TttkvNnlrmqgrvyOqpr-Ge-NRl9WJDYro-A130_assertion
a
np:Assertion
.
dgn-np:NP666671.RAS01yjRx4TttkvNnlrmqgrvyOqpr-Ge-NRl9WJDYro-A130_provenance
a
np:Provenance
.
dgn-np:NP666671.RAS01yjRx4TttkvNnlrmqgrvyOqpr-Ge-NRl9WJDYro-A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP666671.RAS01yjRx4TttkvNnlrmqgrvyOqpr-Ge-NRl9WJDYro-A130_assertion
{
miriam-gene:3126
a
ncit:C16612
.
lld:C0543698
a
ncit:C7057
.
dgn-gda:DGN1e20e044778d01ce7c2989f2baaaba52
sio:SIO_000628
miriam-gene:3126
,
lld:C0543698
;
a
sio:SIO_001121
.
}
dgn-np:NP666671.RAS01yjRx4TttkvNnlrmqgrvyOqpr-Ge-NRl9WJDYro-A130_provenance
{
dgn-np:NP666671.RAS01yjRx4TttkvNnlrmqgrvyOqpr-Ge-NRl9WJDYro-A130_assertion
dcterms:description
"[The clinical characteristics of FT1D with DIHS were similar to those without DIHS except for the high frequency of HLA B62, which may be involved in the pathogenesis of FT1D with DIHS.]. 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:23071161
;
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:NP666671.RAS01yjRx4TttkvNnlrmqgrvyOqpr-Ge-NRl9WJDYro-A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:42+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" .
}