@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP707968.RA2oqTizszbqks0461HlvAxIL4S2PuJxtV4I_jwIx5Fmo
> .
@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:NP707968.RA2oqTizszbqks0461HlvAxIL4S2PuJxtV4I_jwIx5Fmo130_head
{
this:
np:hasAssertion
dgn-np:NP707968.RA2oqTizszbqks0461HlvAxIL4S2PuJxtV4I_jwIx5Fmo130_assertion
;
np:hasProvenance
dgn-np:NP707968.RA2oqTizszbqks0461HlvAxIL4S2PuJxtV4I_jwIx5Fmo130_provenance
;
np:hasPublicationInfo
dgn-np:NP707968.RA2oqTizszbqks0461HlvAxIL4S2PuJxtV4I_jwIx5Fmo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP707968.RA2oqTizszbqks0461HlvAxIL4S2PuJxtV4I_jwIx5Fmo130_assertion
a
np:Assertion
.
dgn-np:NP707968.RA2oqTizszbqks0461HlvAxIL4S2PuJxtV4I_jwIx5Fmo130_provenance
a
np:Provenance
.
dgn-np:NP707968.RA2oqTizszbqks0461HlvAxIL4S2PuJxtV4I_jwIx5Fmo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP707968.RA2oqTizszbqks0461HlvAxIL4S2PuJxtV4I_jwIx5Fmo130_assertion
{
miriam-gene:4878
a
ncit:C16612
.
lld:C2931674
a
ncit:C7057
.
dgn-gda:DGN6e6ce9bf4cb6b7eb0f7db17d856a6e5d
sio:SIO_000628
miriam-gene:4878
,
lld:C2931674
;
a
sio:SIO_001121
.
}
dgn-np:NP707968.RA2oqTizszbqks0461HlvAxIL4S2PuJxtV4I_jwIx5Fmo130_provenance
{
dgn-np:NP707968.RA2oqTizszbqks0461HlvAxIL4S2PuJxtV4I_jwIx5Fmo130_assertion
dcterms:description
"[Severity of Batten disease due to mutations in CLN3 and the degree of ANP resistance in yeast are related when the equivalent amino acid replacements in Cln3p and Btn1p are compared.]. 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:10191120
;
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:NP707968.RA2oqTizszbqks0461HlvAxIL4S2PuJxtV4I_jwIx5Fmo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:10+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" .
}