@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP798624.RA9yJ0jswt_bgOx-zQDVT2pe1DIWXL2usZy-3VEbx_TLw
> .
@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:NP798624.RA9yJ0jswt_bgOx-zQDVT2pe1DIWXL2usZy-3VEbx_TLw130_head
{
this:
np:hasAssertion
dgn-np:NP798624.RA9yJ0jswt_bgOx-zQDVT2pe1DIWXL2usZy-3VEbx_TLw130_assertion
;
np:hasProvenance
dgn-np:NP798624.RA9yJ0jswt_bgOx-zQDVT2pe1DIWXL2usZy-3VEbx_TLw130_provenance
;
np:hasPublicationInfo
dgn-np:NP798624.RA9yJ0jswt_bgOx-zQDVT2pe1DIWXL2usZy-3VEbx_TLw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP798624.RA9yJ0jswt_bgOx-zQDVT2pe1DIWXL2usZy-3VEbx_TLw130_assertion
a
np:Assertion
.
dgn-np:NP798624.RA9yJ0jswt_bgOx-zQDVT2pe1DIWXL2usZy-3VEbx_TLw130_provenance
a
np:Provenance
.
dgn-np:NP798624.RA9yJ0jswt_bgOx-zQDVT2pe1DIWXL2usZy-3VEbx_TLw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP798624.RA9yJ0jswt_bgOx-zQDVT2pe1DIWXL2usZy-3VEbx_TLw130_assertion
{
miriam-gene:65125
a
ncit:C16612
.
lld:C0699739
a
ncit:C7057
.
dgn-gda:DGN558542f7c8f16e3a739d32817665a2a5
sio:SIO_000628
miriam-gene:65125
,
lld:C0699739
;
a
sio:SIO_001121
.
}
dgn-np:NP798624.RA9yJ0jswt_bgOx-zQDVT2pe1DIWXL2usZy-3VEbx_TLw130_provenance
{
dgn-np:NP798624.RA9yJ0jswt_bgOx-zQDVT2pe1DIWXL2usZy-3VEbx_TLw130_assertion
dcterms:description
"[The segregation of polymorphic alleles at and around loci for p75NGFR, TRKA, TRKB, BDNF, and familial dysautonomia (another hereditary sensory neuropathy having features in common with HSN II) virtually excluded these genes as the cause of HSN II in this family.]. 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:8895241
;
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:NP798624.RA9yJ0jswt_bgOx-zQDVT2pe1DIWXL2usZy-3VEbx_TLw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:10+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" .
}