@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP399959.RAlDpUhP_QGiKnsVNVXyAuaKW_uomuyx-WI8S-qkUOw3A
> .
@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:NP399959.RAlDpUhP_QGiKnsVNVXyAuaKW_uomuyx-WI8S-qkUOw3A130_head
{
this:
np:hasAssertion
dgn-np:NP399959.RAlDpUhP_QGiKnsVNVXyAuaKW_uomuyx-WI8S-qkUOw3A130_assertion
;
np:hasProvenance
dgn-np:NP399959.RAlDpUhP_QGiKnsVNVXyAuaKW_uomuyx-WI8S-qkUOw3A130_provenance
;
np:hasPublicationInfo
dgn-np:NP399959.RAlDpUhP_QGiKnsVNVXyAuaKW_uomuyx-WI8S-qkUOw3A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP399959.RAlDpUhP_QGiKnsVNVXyAuaKW_uomuyx-WI8S-qkUOw3A130_assertion
a
np:Assertion
.
dgn-np:NP399959.RAlDpUhP_QGiKnsVNVXyAuaKW_uomuyx-WI8S-qkUOw3A130_provenance
a
np:Provenance
.
dgn-np:NP399959.RAlDpUhP_QGiKnsVNVXyAuaKW_uomuyx-WI8S-qkUOw3A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP399959.RAlDpUhP_QGiKnsVNVXyAuaKW_uomuyx-WI8S-qkUOw3A130_assertion
{
miriam-gene:1509
a
ncit:C16612
.
lld:C0027877
a
ncit:C7057
.
dgn-gda:DGN21257d581963626d7bebfa90cdbea844
sio:SIO_000628
miriam-gene:1509
,
lld:C0027877
;
a
sio:SIO_001121
.
}
dgn-np:NP399959.RAlDpUhP_QGiKnsVNVXyAuaKW_uomuyx-WI8S-qkUOw3A130_provenance
{
dgn-np:NP399959.RAlDpUhP_QGiKnsVNVXyAuaKW_uomuyx-WI8S-qkUOw3A130_assertion
dcterms:description
"[Although functions are defined for some of the soluble proteins that are defective in NCL (cathepsin D, PPT1, and TPP1), the primary function of the other proteins defective in NCLs (CLN3, CLN5, CLN6, CLN7, and CLN8) remain poorly defined.]. 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:20680390
;
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:NP399959.RAlDpUhP_QGiKnsVNVXyAuaKW_uomuyx-WI8S-qkUOw3A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:58+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" .
}