@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP469876.RA0Co32g3st7vLmeltT-EhR0zNGddoARPxnyczSrNisOE
> .
@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:NP469876.RA0Co32g3st7vLmeltT-EhR0zNGddoARPxnyczSrNisOE130_head
{
this:
np:hasAssertion
dgn-np:NP469876.RA0Co32g3st7vLmeltT-EhR0zNGddoARPxnyczSrNisOE130_assertion
;
np:hasProvenance
dgn-np:NP469876.RA0Co32g3st7vLmeltT-EhR0zNGddoARPxnyczSrNisOE130_provenance
;
np:hasPublicationInfo
dgn-np:NP469876.RA0Co32g3st7vLmeltT-EhR0zNGddoARPxnyczSrNisOE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP469876.RA0Co32g3st7vLmeltT-EhR0zNGddoARPxnyczSrNisOE130_assertion
a
np:Assertion
.
dgn-np:NP469876.RA0Co32g3st7vLmeltT-EhR0zNGddoARPxnyczSrNisOE130_provenance
a
np:Provenance
.
dgn-np:NP469876.RA0Co32g3st7vLmeltT-EhR0zNGddoARPxnyczSrNisOE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP469876.RA0Co32g3st7vLmeltT-EhR0zNGddoARPxnyczSrNisOE130_assertion
{
miriam-gene:5827
a
ncit:C16612
.
lld:C0393814
a
ncit:C7057
.
dgn-gda:DGN7724c37aae75dcc942652968a5813267
sio:SIO_000628
miriam-gene:5827
,
lld:C0393814
;
a
sio:SIO_001121
.
}
dgn-np:NP469876.RA0Co32g3st7vLmeltT-EhR0zNGddoARPxnyczSrNisOE130_provenance
{
dgn-np:NP469876.RA0Co32g3st7vLmeltT-EhR0zNGddoARPxnyczSrNisOE130_assertion
dcterms:description
"[Therefore, such MPZ gene mutations should be searched for in cases of demyelinating neuropathy with acute nerve compression as well as in cases of the HNPP phenotype associated with normal the PMP22 gene.]. 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:18663734
;
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:NP469876.RA0Co32g3st7vLmeltT-EhR0zNGddoARPxnyczSrNisOE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:41+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" .
}