@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP416913.RA6HwmyQl2YRxZJ9qUYKFihneNdhe2replU8QgdZoTLq0
> .
@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:NP416913.RA6HwmyQl2YRxZJ9qUYKFihneNdhe2replU8QgdZoTLq0130_head
{
this:
np:hasAssertion
dgn-np:NP416913.RA6HwmyQl2YRxZJ9qUYKFihneNdhe2replU8QgdZoTLq0130_assertion
;
np:hasProvenance
dgn-np:NP416913.RA6HwmyQl2YRxZJ9qUYKFihneNdhe2replU8QgdZoTLq0130_provenance
;
np:hasPublicationInfo
dgn-np:NP416913.RA6HwmyQl2YRxZJ9qUYKFihneNdhe2replU8QgdZoTLq0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP416913.RA6HwmyQl2YRxZJ9qUYKFihneNdhe2replU8QgdZoTLq0130_assertion
a
np:Assertion
.
dgn-np:NP416913.RA6HwmyQl2YRxZJ9qUYKFihneNdhe2replU8QgdZoTLq0130_provenance
a
np:Provenance
.
dgn-np:NP416913.RA6HwmyQl2YRxZJ9qUYKFihneNdhe2replU8QgdZoTLq0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP416913.RA6HwmyQl2YRxZJ9qUYKFihneNdhe2replU8QgdZoTLq0130_assertion
{
miriam-gene:1716
a
ncit:C16612
.
lld:C0085584
a
ncit:C7057
.
dgn-gda:DGN9748ae955a7c27cc1a37473aac039235
sio:SIO_000628
miriam-gene:1716
,
lld:C0085584
;
a
sio:SIO_001121
.
}
dgn-np:NP416913.RA6HwmyQl2YRxZJ9qUYKFihneNdhe2replU8QgdZoTLq0130_provenance
{
dgn-np:NP416913.RA6HwmyQl2YRxZJ9qUYKFihneNdhe2replU8QgdZoTLq0130_assertion
dcterms:description
"[The phenotype was distinctive for each gene, with hepatic failure and encephalopathy associated with mutations in the deoxyguanosine kinase gene and isolated devastating myopathy as the sole manifestation of thymidine kinase 2 deficiency.]. 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:12110944
;
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:NP416913.RA6HwmyQl2YRxZJ9qUYKFihneNdhe2replU8QgdZoTLq0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:07+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" .
}