@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP398990.RA3GswMvY04M4lWny3My9pS3U6Z0D2wSBCogImialCXTc
> .
@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:NP398990.RA3GswMvY04M4lWny3My9pS3U6Z0D2wSBCogImialCXTc130_head
{
this:
np:hasAssertion
dgn-np:NP398990.RA3GswMvY04M4lWny3My9pS3U6Z0D2wSBCogImialCXTc130_assertion
;
np:hasProvenance
dgn-np:NP398990.RA3GswMvY04M4lWny3My9pS3U6Z0D2wSBCogImialCXTc130_provenance
;
np:hasPublicationInfo
dgn-np:NP398990.RA3GswMvY04M4lWny3My9pS3U6Z0D2wSBCogImialCXTc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP398990.RA3GswMvY04M4lWny3My9pS3U6Z0D2wSBCogImialCXTc130_assertion
a
np:Assertion
.
dgn-np:NP398990.RA3GswMvY04M4lWny3My9pS3U6Z0D2wSBCogImialCXTc130_provenance
a
np:Provenance
.
dgn-np:NP398990.RA3GswMvY04M4lWny3My9pS3U6Z0D2wSBCogImialCXTc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP398990.RA3GswMvY04M4lWny3My9pS3U6Z0D2wSBCogImialCXTc130_assertion
{
miriam-gene:3908
a
ncit:C16612
.
lld:C0026848
a
ncit:C7057
.
dgn-gda:DGN17642b81e727bc856cc36158ef6564fa
sio:SIO_000628
miriam-gene:3908
,
lld:C0026848
;
a
sio:SIO_001121
.
}
dgn-np:NP398990.RA3GswMvY04M4lWny3My9pS3U6Z0D2wSBCogImialCXTc130_provenance
{
dgn-np:NP398990.RA3GswMvY04M4lWny3My9pS3U6Z0D2wSBCogImialCXTc130_assertion
dcterms:description
"[A 20-year-old man with mild myopathy, external ophthalmoparesis, epilepsy, and diffuse white matter hyperintensity in the brain on magnetic resonance imaging had partial merosin deficiency in muscle and absent merosin in the endoneurium.]. 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:12661054
;
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:NP398990.RA3GswMvY04M4lWny3My9pS3U6Z0D2wSBCogImialCXTc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:57+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" .
}