@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP422857.RAtwevyOBr_kOJRGLJypXA6j9wbQx_oWNRm1bv5_bSfF0
> .
@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:NP422857.RAtwevyOBr_kOJRGLJypXA6j9wbQx_oWNRm1bv5_bSfF0130_head
{
this:
np:hasAssertion
dgn-np:NP422857.RAtwevyOBr_kOJRGLJypXA6j9wbQx_oWNRm1bv5_bSfF0130_assertion
;
np:hasProvenance
dgn-np:NP422857.RAtwevyOBr_kOJRGLJypXA6j9wbQx_oWNRm1bv5_bSfF0130_provenance
;
np:hasPublicationInfo
dgn-np:NP422857.RAtwevyOBr_kOJRGLJypXA6j9wbQx_oWNRm1bv5_bSfF0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP422857.RAtwevyOBr_kOJRGLJypXA6j9wbQx_oWNRm1bv5_bSfF0130_assertion
a
np:Assertion
.
dgn-np:NP422857.RAtwevyOBr_kOJRGLJypXA6j9wbQx_oWNRm1bv5_bSfF0130_provenance
a
np:Provenance
.
dgn-np:NP422857.RAtwevyOBr_kOJRGLJypXA6j9wbQx_oWNRm1bv5_bSfF0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP422857.RAtwevyOBr_kOJRGLJypXA6j9wbQx_oWNRm1bv5_bSfF0130_assertion
{
miriam-gene:1509
a
ncit:C16612
.
lld:C0027877
a
ncit:C7057
.
dgn-gda:DGNe0e3b7c11d540d12328f85082a6de95f
sio:SIO_000628
miriam-gene:1509
,
lld:C0027877
;
a
sio:SIO_001121
.
}
dgn-np:NP422857.RAtwevyOBr_kOJRGLJypXA6j9wbQx_oWNRm1bv5_bSfF0130_provenance
{
dgn-np:NP422857.RAtwevyOBr_kOJRGLJypXA6j9wbQx_oWNRm1bv5_bSfF0130_assertion
dcterms:description
"[Among the fourteen different forms of NCL described to date, CLN1 and CLN10 are marked by granular lipopigments, CLN2 by curvilinear profiles (CVPs), CLN3 by fingerprint profiles (FPPs), and other forms by a combination of these 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:23200925
;
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:NP422857.RAtwevyOBr_kOJRGLJypXA6j9wbQx_oWNRm1bv5_bSfF0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:11+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" .
}