@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP580143.RA5l2eh2REqls4_JiwstCjM1NvDQ7OdWPJxM8Kct_0Iho
> .
@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:NP580143.RA5l2eh2REqls4_JiwstCjM1NvDQ7OdWPJxM8Kct_0Iho130_head
{
this:
np:hasAssertion
dgn-np:NP580143.RA5l2eh2REqls4_JiwstCjM1NvDQ7OdWPJxM8Kct_0Iho130_assertion
;
np:hasProvenance
dgn-np:NP580143.RA5l2eh2REqls4_JiwstCjM1NvDQ7OdWPJxM8Kct_0Iho130_provenance
;
np:hasPublicationInfo
dgn-np:NP580143.RA5l2eh2REqls4_JiwstCjM1NvDQ7OdWPJxM8Kct_0Iho130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP580143.RA5l2eh2REqls4_JiwstCjM1NvDQ7OdWPJxM8Kct_0Iho130_assertion
a
np:Assertion
.
dgn-np:NP580143.RA5l2eh2REqls4_JiwstCjM1NvDQ7OdWPJxM8Kct_0Iho130_provenance
a
np:Provenance
.
dgn-np:NP580143.RA5l2eh2REqls4_JiwstCjM1NvDQ7OdWPJxM8Kct_0Iho130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP580143.RA5l2eh2REqls4_JiwstCjM1NvDQ7OdWPJxM8Kct_0Iho130_assertion
{
miriam-gene:5354
a
ncit:C16612
.
lld:C0751604
a
ncit:C7057
.
dgn-gda:DGNd6eabe810ef62eddb836ad9a2b53912c
sio:SIO_000628
miriam-gene:5354
,
lld:C0751604
;
a
sio:SIO_001122
.
}
dgn-np:NP580143.RA5l2eh2REqls4_JiwstCjM1NvDQ7OdWPJxM8Kct_0Iho130_provenance
{
dgn-np:NP580143.RA5l2eh2REqls4_JiwstCjM1NvDQ7OdWPJxM8Kct_0Iho130_assertion
dcterms:description
"[The disease spectrum for PMD and SPG2 is extraordinarily broad and can be best understood by accounting not only for the wide range of mutations that can occur but also for the effects of PLP1 mutations on both cell autonomous and non-cell autonomous processes in myelinating cells.]. 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:17115121
;
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:NP580143.RA5l2eh2REqls4_JiwstCjM1NvDQ7OdWPJxM8Kct_0Iho130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:08+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" .
}