@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP760083.RADFqIuJaNtmgcD66M_CzSb7pOfz4RBDWEknO_g7PKgII
> .
@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:NP760083.RADFqIuJaNtmgcD66M_CzSb7pOfz4RBDWEknO_g7PKgII130_head
{
this:
np:hasAssertion
dgn-np:NP760083.RADFqIuJaNtmgcD66M_CzSb7pOfz4RBDWEknO_g7PKgII130_assertion
;
np:hasProvenance
dgn-np:NP760083.RADFqIuJaNtmgcD66M_CzSb7pOfz4RBDWEknO_g7PKgII130_provenance
;
np:hasPublicationInfo
dgn-np:NP760083.RADFqIuJaNtmgcD66M_CzSb7pOfz4RBDWEknO_g7PKgII130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP760083.RADFqIuJaNtmgcD66M_CzSb7pOfz4RBDWEknO_g7PKgII130_assertion
a
np:Assertion
.
dgn-np:NP760083.RADFqIuJaNtmgcD66M_CzSb7pOfz4RBDWEknO_g7PKgII130_provenance
a
np:Provenance
.
dgn-np:NP760083.RADFqIuJaNtmgcD66M_CzSb7pOfz4RBDWEknO_g7PKgII130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP760083.RADFqIuJaNtmgcD66M_CzSb7pOfz4RBDWEknO_g7PKgII130_assertion
{
miriam-gene:3048
a
ncit:C16612
.
lld:C1263721
a
ncit:C7057
.
dgn-gda:DGN806f802e8db71e4e6d89c20e4fab1a0a
sio:SIO_000628
miriam-gene:3048
,
lld:C1263721
;
a
sio:SIO_001121
.
}
dgn-np:NP760083.RADFqIuJaNtmgcD66M_CzSb7pOfz4RBDWEknO_g7PKgII130_provenance
{
dgn-np:NP760083.RADFqIuJaNtmgcD66M_CzSb7pOfz4RBDWEknO_g7PKgII130_assertion
dcterms:description
"[Five years later, Quentin Gibson (then of Queen's University, Belfast, Ireland) correctly identified the pathway involved in the reduction of methemoglobin in the family, thereby describing the first hereditary trait involving a specific enzyme 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:12393396
;
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:NP760083.RADFqIuJaNtmgcD66M_CzSb7pOfz4RBDWEknO_g7PKgII130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:40+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" .
}