@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP285616.RAhdvPgmrc827ryvRbAcM-wmAHo-UDvQLFUrYKLpQ4nl8
> .
@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:NP285616.RAhdvPgmrc827ryvRbAcM-wmAHo-UDvQLFUrYKLpQ4nl8130_head
{
this:
np:hasAssertion
dgn-np:NP285616.RAhdvPgmrc827ryvRbAcM-wmAHo-UDvQLFUrYKLpQ4nl8130_assertion
;
np:hasProvenance
dgn-np:NP285616.RAhdvPgmrc827ryvRbAcM-wmAHo-UDvQLFUrYKLpQ4nl8130_provenance
;
np:hasPublicationInfo
dgn-np:NP285616.RAhdvPgmrc827ryvRbAcM-wmAHo-UDvQLFUrYKLpQ4nl8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP285616.RAhdvPgmrc827ryvRbAcM-wmAHo-UDvQLFUrYKLpQ4nl8130_assertion
a
np:Assertion
.
dgn-np:NP285616.RAhdvPgmrc827ryvRbAcM-wmAHo-UDvQLFUrYKLpQ4nl8130_provenance
a
np:Provenance
.
dgn-np:NP285616.RAhdvPgmrc827ryvRbAcM-wmAHo-UDvQLFUrYKLpQ4nl8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP285616.RAhdvPgmrc827ryvRbAcM-wmAHo-UDvQLFUrYKLpQ4nl8130_assertion
{
miriam-gene:59341
a
ncit:C16612
.
lld:C0442874
a
ncit:C7057
.
dgn-gda:DGNd34546572ab9bf8ff59d95a4ae0ea816
sio:SIO_000628
miriam-gene:59341
,
lld:C0442874
;
a
sio:SIO_001121
.
}
dgn-np:NP285616.RAhdvPgmrc827ryvRbAcM-wmAHo-UDvQLFUrYKLpQ4nl8130_provenance
{
dgn-np:NP285616.RAhdvPgmrc827ryvRbAcM-wmAHo-UDvQLFUrYKLpQ4nl8130_assertion
dcterms:description
"[Recent studies reported that mutations in TRPV4, including some in its ankyrin repeat domain (ARD), are associated with human inherited diseases, including neuropathies and skeletal dysplasias, probably because of the increased constitutive activity of the channel.]. 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:22702953
;
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:NP285616.RAhdvPgmrc827ryvRbAcM-wmAHo-UDvQLFUrYKLpQ4nl8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:41+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" .
}