@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP910394.RAdR45RRiOOjZiyMPKItLFY89D7FLQ-n39EUX-7WTMUbU
> .
@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:NP910394.RAdR45RRiOOjZiyMPKItLFY89D7FLQ-n39EUX-7WTMUbU130_head
{
this:
np:hasAssertion
dgn-np:NP910394.RAdR45RRiOOjZiyMPKItLFY89D7FLQ-n39EUX-7WTMUbU130_assertion
;
np:hasProvenance
dgn-np:NP910394.RAdR45RRiOOjZiyMPKItLFY89D7FLQ-n39EUX-7WTMUbU130_provenance
;
np:hasPublicationInfo
dgn-np:NP910394.RAdR45RRiOOjZiyMPKItLFY89D7FLQ-n39EUX-7WTMUbU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP910394.RAdR45RRiOOjZiyMPKItLFY89D7FLQ-n39EUX-7WTMUbU130_assertion
a
np:Assertion
.
dgn-np:NP910394.RAdR45RRiOOjZiyMPKItLFY89D7FLQ-n39EUX-7WTMUbU130_provenance
a
np:Provenance
.
dgn-np:NP910394.RAdR45RRiOOjZiyMPKItLFY89D7FLQ-n39EUX-7WTMUbU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP910394.RAdR45RRiOOjZiyMPKItLFY89D7FLQ-n39EUX-7WTMUbU130_assertion
{
miriam-gene:9519
a
ncit:C16612
.
lld:C0238286
a
ncit:C7057
.
dgn-gda:DGN54b610ebe0a59556671f038962570b9a
sio:SIO_000628
miriam-gene:9519
,
lld:C0238286
;
a
sio:SIO_001121
.
}
dgn-np:NP910394.RAdR45RRiOOjZiyMPKItLFY89D7FLQ-n39EUX-7WTMUbU130_provenance
{
dgn-np:NP910394.RAdR45RRiOOjZiyMPKItLFY89D7FLQ-n39EUX-7WTMUbU130_assertion
dcterms:description
"[The list of confirmed 'channelopathies' is growing and several members of the TRP family of ion channels have been implicated in human diseases such as mucolipidosis type IV (MLIV), autosomal dominant polycystic kidney disease (ADPKD), familial focal segmental glomerulosclerosis (FSG), hypomagnesemia with secondary hypocalcaemia (HSH), and several forms of cancer.]. 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:17138610
;
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:NP910394.RAdR45RRiOOjZiyMPKItLFY89D7FLQ-n39EUX-7WTMUbU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:19+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" .
}