@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP237910.RAWUdcbh3p9VOuAic9QkVaFOyL2u725t0vUnpNGRc6Sdc
> .
@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:NP237910.RAWUdcbh3p9VOuAic9QkVaFOyL2u725t0vUnpNGRc6Sdc130_head
{
this:
np:hasAssertion
dgn-np:NP237910.RAWUdcbh3p9VOuAic9QkVaFOyL2u725t0vUnpNGRc6Sdc130_assertion
;
np:hasProvenance
dgn-np:NP237910.RAWUdcbh3p9VOuAic9QkVaFOyL2u725t0vUnpNGRc6Sdc130_provenance
;
np:hasPublicationInfo
dgn-np:NP237910.RAWUdcbh3p9VOuAic9QkVaFOyL2u725t0vUnpNGRc6Sdc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP237910.RAWUdcbh3p9VOuAic9QkVaFOyL2u725t0vUnpNGRc6Sdc130_assertion
a
np:Assertion
.
dgn-np:NP237910.RAWUdcbh3p9VOuAic9QkVaFOyL2u725t0vUnpNGRc6Sdc130_provenance
a
np:Provenance
.
dgn-np:NP237910.RAWUdcbh3p9VOuAic9QkVaFOyL2u725t0vUnpNGRc6Sdc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP237910.RAWUdcbh3p9VOuAic9QkVaFOyL2u725t0vUnpNGRc6Sdc130_assertion
{
miriam-gene:8291
a
ncit:C16612
.
lld:C1850808
a
ncit:C7057
.
dgn-gda:DGN965cd037a40800f7d2e65e1ec1bb68dd
sio:SIO_000628
miriam-gene:8291
,
lld:C1850808
;
a
sio:SIO_001121
.
}
dgn-np:NP237910.RAWUdcbh3p9VOuAic9QkVaFOyL2u725t0vUnpNGRc6Sdc130_provenance
{
dgn-np:NP237910.RAWUdcbh3p9VOuAic9QkVaFOyL2u725t0vUnpNGRc6Sdc130_assertion
dcterms:description
"[Although MM patients and their mutations in the DYSF gene have been found from all over the world, there is only one report of genetically confirmed case of MM in Korea.]. 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:16891820
;
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:NP237910.RAWUdcbh3p9VOuAic9QkVaFOyL2u725t0vUnpNGRc6Sdc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:13+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" .
}