@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP662196.RAdnToUnPhcYEEdPPKfReZDp-cz1DNNVCxfJCkWhF1-xs
> .
@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/v3.0.0/void/
> .
dgn-np:NP662196.RAdnToUnPhcYEEdPPKfReZDp-cz1DNNVCxfJCkWhF1-xs130_head
{
this:
np:hasAssertion
dgn-np:NP662196.RAdnToUnPhcYEEdPPKfReZDp-cz1DNNVCxfJCkWhF1-xs130_assertion
;
np:hasProvenance
dgn-np:NP662196.RAdnToUnPhcYEEdPPKfReZDp-cz1DNNVCxfJCkWhF1-xs130_provenance
;
np:hasPublicationInfo
dgn-np:NP662196.RAdnToUnPhcYEEdPPKfReZDp-cz1DNNVCxfJCkWhF1-xs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP662196.RAdnToUnPhcYEEdPPKfReZDp-cz1DNNVCxfJCkWhF1-xs130_assertion
a
np:Assertion
.
dgn-np:NP662196.RAdnToUnPhcYEEdPPKfReZDp-cz1DNNVCxfJCkWhF1-xs130_provenance
a
np:Provenance
.
dgn-np:NP662196.RAdnToUnPhcYEEdPPKfReZDp-cz1DNNVCxfJCkWhF1-xs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP662196.RAdnToUnPhcYEEdPPKfReZDp-cz1DNNVCxfJCkWhF1-xs130_assertion
{
miriam-gene:5827
a
ncit:C16612
.
lld:C0027888
a
ncit:C7057
.
dgn-gda:DGNdac6381fbd85f6b711ec3ecfc50789ad
sio:SIO_000628
miriam-gene:5827
,
lld:C0027888
;
a
sio:SIO_001121
.
}
dgn-np:NP662196.RAdnToUnPhcYEEdPPKfReZDp-cz1DNNVCxfJCkWhF1-xs130_provenance
{
dgn-np:NP662196.RAdnToUnPhcYEEdPPKfReZDp-cz1DNNVCxfJCkWhF1-xs130_assertion
dcterms:description
"[It now appears that most of the HMSNs are related to mutations affecting genes encoding Schwann cell proteins, specifically the Peripheral Myelin Protein PMP22, Myelin Protein Zero, and one of the gap junction proteins, connexin-32.]. 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:8520723
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP662196.RAdnToUnPhcYEEdPPKfReZDp-cz1DNNVCxfJCkWhF1-xs130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:44:17+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}