@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1386362.RAaZaPi7S76-IZ7onobiBy82ux3YMn4BNrAmVZKxgwIRI
> .
@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:NP1386362.RAaZaPi7S76-IZ7onobiBy82ux3YMn4BNrAmVZKxgwIRI130_head
{
this:
np:hasAssertion
dgn-np:NP1386362.RAaZaPi7S76-IZ7onobiBy82ux3YMn4BNrAmVZKxgwIRI130_assertion
;
np:hasProvenance
dgn-np:NP1386362.RAaZaPi7S76-IZ7onobiBy82ux3YMn4BNrAmVZKxgwIRI130_provenance
;
np:hasPublicationInfo
dgn-np:NP1386362.RAaZaPi7S76-IZ7onobiBy82ux3YMn4BNrAmVZKxgwIRI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1386362.RAaZaPi7S76-IZ7onobiBy82ux3YMn4BNrAmVZKxgwIRI130_assertion
a
np:Assertion
.
dgn-np:NP1386362.RAaZaPi7S76-IZ7onobiBy82ux3YMn4BNrAmVZKxgwIRI130_provenance
a
np:Provenance
.
dgn-np:NP1386362.RAaZaPi7S76-IZ7onobiBy82ux3YMn4BNrAmVZKxgwIRI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1386362.RAaZaPi7S76-IZ7onobiBy82ux3YMn4BNrAmVZKxgwIRI130_assertion
{
miriam-gene:2705
a
ncit:C16612
.
lld:C0393808
a
ncit:C7057
.
dgn-gda:DGN818030d80e60a46b4b353898f1507032
sio:SIO_000628
miriam-gene:2705
,
lld:C0393808
;
a
sio:SIO_001121
.
}
dgn-np:NP1386362.RAaZaPi7S76-IZ7onobiBy82ux3YMn4BNrAmVZKxgwIRI130_provenance
{
dgn-np:NP1386362.RAaZaPi7S76-IZ7onobiBy82ux3YMn4BNrAmVZKxgwIRI130_assertion
dcterms:description
"[In addition, engineered mutants heterozygously or homozygously deficient in the myelin component P0 show the pathology of distinct CMT1B and DS patients, respectively, while Cx32 deficient mice develop pathological abnormalities similar to those of CMTX patients.]. 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:9418989
;
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:NP1386362.RAaZaPi7S76-IZ7onobiBy82ux3YMn4BNrAmVZKxgwIRI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:14+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" .
}