@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1151906.RAUxLtwRiqXuQmx2yW-4uLmFSoEppSJTx3PCu7OJ86c8k
> .
@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/v4.0.0/void/
> .
dgn-np:NP1151906.RAUxLtwRiqXuQmx2yW-4uLmFSoEppSJTx3PCu7OJ86c8k130_head
{
this:
np:hasAssertion
dgn-np:NP1151906.RAUxLtwRiqXuQmx2yW-4uLmFSoEppSJTx3PCu7OJ86c8k130_assertion
;
np:hasProvenance
dgn-np:NP1151906.RAUxLtwRiqXuQmx2yW-4uLmFSoEppSJTx3PCu7OJ86c8k130_provenance
;
np:hasPublicationInfo
dgn-np:NP1151906.RAUxLtwRiqXuQmx2yW-4uLmFSoEppSJTx3PCu7OJ86c8k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1151906.RAUxLtwRiqXuQmx2yW-4uLmFSoEppSJTx3PCu7OJ86c8k130_assertion
a
np:Assertion
.
dgn-np:NP1151906.RAUxLtwRiqXuQmx2yW-4uLmFSoEppSJTx3PCu7OJ86c8k130_provenance
a
np:Provenance
.
dgn-np:NP1151906.RAUxLtwRiqXuQmx2yW-4uLmFSoEppSJTx3PCu7OJ86c8k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1151906.RAUxLtwRiqXuQmx2yW-4uLmFSoEppSJTx3PCu7OJ86c8k130_assertion
{
miriam-gene:4914
a
ncit:C16612
.
lld:C0025362
a
ncit:C7057
.
dgn-gda:DGN5fe034b3fe030b91ddb788a745254585
sio:SIO_000628
miriam-gene:4914
,
lld:C0025362
;
a
sio:SIO_001121
.
}
dgn-np:NP1151906.RAUxLtwRiqXuQmx2yW-4uLmFSoEppSJTx3PCu7OJ86c8k130_provenance
{
dgn-np:NP1151906.RAUxLtwRiqXuQmx2yW-4uLmFSoEppSJTx3PCu7OJ86c8k130_assertion
dcterms:description
"[Interestingly, alterations in NGF signalling, due to mutations in the NGF TRKA gene, have also been involved in another congenital insensitivity to pain, HSAN IV, characterized not only by absence of reaction to painful stimuli, but also anhidrosis and mental retardation.]. 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:24494679
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1151906.RAUxLtwRiqXuQmx2yW-4uLmFSoEppSJTx3PCu7OJ86c8k130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:28+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: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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}