@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP64329.RA_kDKu4KFWZ5p72dZ1Fe001QZtgn4YDPSlDGQLE1XBxU
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP64329.RA_kDKu4KFWZ5p72dZ1Fe001QZtgn4YDPSlDGQLE1XBxU130_head
{
this:
np:hasAssertion
dgn-np:NP64329.RA_kDKu4KFWZ5p72dZ1Fe001QZtgn4YDPSlDGQLE1XBxU130_assertion
;
np:hasProvenance
dgn-np:NP64329.RA_kDKu4KFWZ5p72dZ1Fe001QZtgn4YDPSlDGQLE1XBxU130_provenance
;
np:hasPublicationInfo
dgn-np:NP64329.RA_kDKu4KFWZ5p72dZ1Fe001QZtgn4YDPSlDGQLE1XBxU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP64329.RA_kDKu4KFWZ5p72dZ1Fe001QZtgn4YDPSlDGQLE1XBxU130_assertion
a
np:Assertion
.
dgn-np:NP64329.RA_kDKu4KFWZ5p72dZ1Fe001QZtgn4YDPSlDGQLE1XBxU130_provenance
a
np:Provenance
.
dgn-np:NP64329.RA_kDKu4KFWZ5p72dZ1Fe001QZtgn4YDPSlDGQLE1XBxU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP64329.RA_kDKu4KFWZ5p72dZ1Fe001QZtgn4YDPSlDGQLE1XBxU130_assertion
{
miriam-gene:6559
a
ncit:C16612
.
lld:C0268450
a
ncit:C7057
.
dgn-gda:DGN44b9620229fb0c24c61e8e4b44d09541
sio:SIO_000628
miriam-gene:6559
,
lld:C0268450
;
a
sio:SIO_001122
.
}
dgn-np:NP64329.RA_kDKu4KFWZ5p72dZ1Fe001QZtgn4YDPSlDGQLE1XBxU130_provenance
{
dgn-np:NP64329.RA_kDKu4KFWZ5p72dZ1Fe001QZtgn4YDPSlDGQLE1XBxU130_assertion
dcterms:description
"[ We found four novel mutations in the NCCT gene in seven Japanese patients with GS. Moreover, our study suggests that the distribution of mutations in the NCCT gene in Japanese GS patients potentially differs from that in other populations.]. 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:15069170
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP64329.RA_kDKu4KFWZ5p72dZ1Fe001QZtgn4YDPSlDGQLE1XBxU130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:15+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}