@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP643624.RAPYQqg_kQq1XNs7Q-PCveq8isAA344hjWzG5ghvhZLJ4
> .
@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:NP643624.RAPYQqg_kQq1XNs7Q-PCveq8isAA344hjWzG5ghvhZLJ4130_head
{
this:
np:hasAssertion
dgn-np:NP643624.RAPYQqg_kQq1XNs7Q-PCveq8isAA344hjWzG5ghvhZLJ4130_assertion
;
np:hasProvenance
dgn-np:NP643624.RAPYQqg_kQq1XNs7Q-PCveq8isAA344hjWzG5ghvhZLJ4130_provenance
;
np:hasPublicationInfo
dgn-np:NP643624.RAPYQqg_kQq1XNs7Q-PCveq8isAA344hjWzG5ghvhZLJ4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP643624.RAPYQqg_kQq1XNs7Q-PCveq8isAA344hjWzG5ghvhZLJ4130_assertion
a
np:Assertion
.
dgn-np:NP643624.RAPYQqg_kQq1XNs7Q-PCveq8isAA344hjWzG5ghvhZLJ4130_provenance
a
np:Provenance
.
dgn-np:NP643624.RAPYQqg_kQq1XNs7Q-PCveq8isAA344hjWzG5ghvhZLJ4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP643624.RAPYQqg_kQq1XNs7Q-PCveq8isAA344hjWzG5ghvhZLJ4130_assertion
{
miriam-gene:4878
a
ncit:C16612
.
lld:C0751383
a
ncit:C7057
.
dgn-gda:DGNb6f55f69e5f60753028d3d12fc3c2837
sio:SIO_000628
miriam-gene:4878
,
lld:C0751383
;
a
sio:SIO_001121
.
}
dgn-np:NP643624.RAPYQqg_kQq1XNs7Q-PCveq8isAA344hjWzG5ghvhZLJ4130_provenance
{
dgn-np:NP643624.RAPYQqg_kQq1XNs7Q-PCveq8isAA344hjWzG5ghvhZLJ4130_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:NP643624.RAPYQqg_kQq1XNs7Q-PCveq8isAA344hjWzG5ghvhZLJ4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:28+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" .
}