@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP673991.RABMT5lshmTYMMWKguqKOBnO2X6s3q_sRqmpRWtBMqoRA
> .
@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:NP673991.RABMT5lshmTYMMWKguqKOBnO2X6s3q_sRqmpRWtBMqoRA130_head
{
this:
np:hasAssertion
dgn-np:NP673991.RABMT5lshmTYMMWKguqKOBnO2X6s3q_sRqmpRWtBMqoRA130_assertion
;
np:hasProvenance
dgn-np:NP673991.RABMT5lshmTYMMWKguqKOBnO2X6s3q_sRqmpRWtBMqoRA130_provenance
;
np:hasPublicationInfo
dgn-np:NP673991.RABMT5lshmTYMMWKguqKOBnO2X6s3q_sRqmpRWtBMqoRA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP673991.RABMT5lshmTYMMWKguqKOBnO2X6s3q_sRqmpRWtBMqoRA130_assertion
a
np:Assertion
.
dgn-np:NP673991.RABMT5lshmTYMMWKguqKOBnO2X6s3q_sRqmpRWtBMqoRA130_provenance
a
np:Provenance
.
dgn-np:NP673991.RABMT5lshmTYMMWKguqKOBnO2X6s3q_sRqmpRWtBMqoRA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP673991.RABMT5lshmTYMMWKguqKOBnO2X6s3q_sRqmpRWtBMqoRA130_assertion
{
miriam-gene:4397
a
ncit:C16612
.
lld:C0038522
a
ncit:C7057
.
dgn-gda:DGN1da98aa98d91a046ae789437f9cb513f
sio:SIO_000628
miriam-gene:4397
,
lld:C0038522
;
a
sio:SIO_001121
.
}
dgn-np:NP673991.RABMT5lshmTYMMWKguqKOBnO2X6s3q_sRqmpRWtBMqoRA130_provenance
{
dgn-np:NP673991.RABMT5lshmTYMMWKguqKOBnO2X6s3q_sRqmpRWtBMqoRA130_assertion
dcterms:description
"[These range from genetic defects that affect lipid metabolism in the leukodystrophies, cytopathic effects of viral infection in SSPE to the action of immunological effector mechanisms in MS and the viral encephalopathies.]. 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:8864286
;
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:NP673991.RABMT5lshmTYMMWKguqKOBnO2X6s3q_sRqmpRWtBMqoRA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:47+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" .
}