@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP449407.RAdCCslZPyTSDyFM4Fq_7nIH-WR_QMxBWFX2hDzu-u4ws
> .
@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:NP449407.RAdCCslZPyTSDyFM4Fq_7nIH-WR_QMxBWFX2hDzu-u4ws130_head
{
this:
np:hasAssertion
dgn-np:NP449407.RAdCCslZPyTSDyFM4Fq_7nIH-WR_QMxBWFX2hDzu-u4ws130_assertion
;
np:hasProvenance
dgn-np:NP449407.RAdCCslZPyTSDyFM4Fq_7nIH-WR_QMxBWFX2hDzu-u4ws130_provenance
;
np:hasPublicationInfo
dgn-np:NP449407.RAdCCslZPyTSDyFM4Fq_7nIH-WR_QMxBWFX2hDzu-u4ws130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP449407.RAdCCslZPyTSDyFM4Fq_7nIH-WR_QMxBWFX2hDzu-u4ws130_assertion
a
np:Assertion
.
dgn-np:NP449407.RAdCCslZPyTSDyFM4Fq_7nIH-WR_QMxBWFX2hDzu-u4ws130_provenance
a
np:Provenance
.
dgn-np:NP449407.RAdCCslZPyTSDyFM4Fq_7nIH-WR_QMxBWFX2hDzu-u4ws130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP449407.RAdCCslZPyTSDyFM4Fq_7nIH-WR_QMxBWFX2hDzu-u4ws130_assertion
{
miriam-gene:6834
a
ncit:C16612
.
lld:C0268237
a
ncit:C7057
.
dgn-gda:DGN930acab1af6017090fe63aa95c674b79
sio:SIO_000628
miriam-gene:6834
,
lld:C0268237
;
a
sio:SIO_001121
.
}
dgn-np:NP449407.RAdCCslZPyTSDyFM4Fq_7nIH-WR_QMxBWFX2hDzu-u4ws130_provenance
{
dgn-np:NP449407.RAdCCslZPyTSDyFM4Fq_7nIH-WR_QMxBWFX2hDzu-u4ws130_assertion
dcterms:description
"[These data confirm that the spectrum of MRI findings in LS is variable and that SURF1 mutations should be considered in patients with encephalomyopathy and COX deficiency even when early MRI findings are negative.]. 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:15214016
;
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:NP449407.RAdCCslZPyTSDyFM4Fq_7nIH-WR_QMxBWFX2hDzu-u4ws130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:08+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" .
}