@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP809619.RAlvdhstXF5aKSKmdWETVevN4zU30hjvvu95-TLjs9P2M
> .
@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:NP809619.RAlvdhstXF5aKSKmdWETVevN4zU30hjvvu95-TLjs9P2M130_head
{
this:
np:hasAssertion
dgn-np:NP809619.RAlvdhstXF5aKSKmdWETVevN4zU30hjvvu95-TLjs9P2M130_assertion
;
np:hasProvenance
dgn-np:NP809619.RAlvdhstXF5aKSKmdWETVevN4zU30hjvvu95-TLjs9P2M130_provenance
;
np:hasPublicationInfo
dgn-np:NP809619.RAlvdhstXF5aKSKmdWETVevN4zU30hjvvu95-TLjs9P2M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP809619.RAlvdhstXF5aKSKmdWETVevN4zU30hjvvu95-TLjs9P2M130_assertion
a
np:Assertion
.
dgn-np:NP809619.RAlvdhstXF5aKSKmdWETVevN4zU30hjvvu95-TLjs9P2M130_provenance
a
np:Provenance
.
dgn-np:NP809619.RAlvdhstXF5aKSKmdWETVevN4zU30hjvvu95-TLjs9P2M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP809619.RAlvdhstXF5aKSKmdWETVevN4zU30hjvvu95-TLjs9P2M130_assertion
{
miriam-gene:7306
a
ncit:C16612
.
lld:C0524851
a
ncit:C7057
.
dgn-gda:DGN636e8ac49ab3ae3cf8f6543094eed48a
sio:SIO_000628
miriam-gene:7306
,
lld:C0524851
;
a
sio:SIO_001121
.
}
dgn-np:NP809619.RAlvdhstXF5aKSKmdWETVevN4zU30hjvvu95-TLjs9P2M130_provenance
{
dgn-np:NP809619.RAlvdhstXF5aKSKmdWETVevN4zU30hjvvu95-TLjs9P2M130_assertion
dcterms:description
"[Mutations in several TRP genes have been implicated in diverse pathological states, including neurodegenerative disorders, skeletal dysplasia, kidney disorders and pain, and ongoing research may help find new therapies for treatments of related diseases.]. 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:21401968
;
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:NP809619.RAlvdhstXF5aKSKmdWETVevN4zU30hjvvu95-TLjs9P2M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:16+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" .
}