@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP222026.RAamNq5_f1lSseB6xiU-iwvZNZYzhnno-o977O3d_2ZRs
> .
@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:NP222026.RAamNq5_f1lSseB6xiU-iwvZNZYzhnno-o977O3d_2ZRs130_head
{
this:
np:hasAssertion
dgn-np:NP222026.RAamNq5_f1lSseB6xiU-iwvZNZYzhnno-o977O3d_2ZRs130_assertion
;
np:hasProvenance
dgn-np:NP222026.RAamNq5_f1lSseB6xiU-iwvZNZYzhnno-o977O3d_2ZRs130_provenance
;
np:hasPublicationInfo
dgn-np:NP222026.RAamNq5_f1lSseB6xiU-iwvZNZYzhnno-o977O3d_2ZRs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP222026.RAamNq5_f1lSseB6xiU-iwvZNZYzhnno-o977O3d_2ZRs130_assertion
a
np:Assertion
.
dgn-np:NP222026.RAamNq5_f1lSseB6xiU-iwvZNZYzhnno-o977O3d_2ZRs130_provenance
a
np:Provenance
.
dgn-np:NP222026.RAamNq5_f1lSseB6xiU-iwvZNZYzhnno-o977O3d_2ZRs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP222026.RAamNq5_f1lSseB6xiU-iwvZNZYzhnno-o977O3d_2ZRs130_assertion
{
miriam-gene:1200
a
ncit:C16612
.
lld:C0027877
a
ncit:C7057
.
dgn-gda:DGN933ad9b5a48ef59178677606dabfc335
sio:SIO_000628
miriam-gene:1200
,
lld:C0027877
;
a
sio:SIO_001121
.
}
dgn-np:NP222026.RAamNq5_f1lSseB6xiU-iwvZNZYzhnno-o977O3d_2ZRs130_provenance
{
dgn-np:NP222026.RAamNq5_f1lSseB6xiU-iwvZNZYzhnno-o977O3d_2ZRs130_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:NP222026.RAamNq5_f1lSseB6xiU-iwvZNZYzhnno-o977O3d_2ZRs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:03+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" .
}