@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP331211.RA-itFtr2SOQUxwNl-IDi5R4zyeCya0iVzHJrI7qotwUA
> .
@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:NP331211.RA-itFtr2SOQUxwNl-IDi5R4zyeCya0iVzHJrI7qotwUA130_head
{
this:
np:hasAssertion
dgn-np:NP331211.RA-itFtr2SOQUxwNl-IDi5R4zyeCya0iVzHJrI7qotwUA130_assertion
;
np:hasProvenance
dgn-np:NP331211.RA-itFtr2SOQUxwNl-IDi5R4zyeCya0iVzHJrI7qotwUA130_provenance
;
np:hasPublicationInfo
dgn-np:NP331211.RA-itFtr2SOQUxwNl-IDi5R4zyeCya0iVzHJrI7qotwUA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP331211.RA-itFtr2SOQUxwNl-IDi5R4zyeCya0iVzHJrI7qotwUA130_assertion
a
np:Assertion
.
dgn-np:NP331211.RA-itFtr2SOQUxwNl-IDi5R4zyeCya0iVzHJrI7qotwUA130_provenance
a
np:Provenance
.
dgn-np:NP331211.RA-itFtr2SOQUxwNl-IDi5R4zyeCya0iVzHJrI7qotwUA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP331211.RA-itFtr2SOQUxwNl-IDi5R4zyeCya0iVzHJrI7qotwUA130_assertion
{
miriam-gene:3982
a
ncit:C16612
.
lld:C0086543
a
ncit:C7057
.
dgn-gda:DGNb80ddca772dc72f9e9130de794002cbe
sio:SIO_000628
miriam-gene:3982
,
lld:C0086543
;
a
sio:SIO_001121
.
}
dgn-np:NP331211.RA-itFtr2SOQUxwNl-IDi5R4zyeCya0iVzHJrI7qotwUA130_provenance
{
dgn-np:NP331211.RA-itFtr2SOQUxwNl-IDi5R4zyeCya0iVzHJrI7qotwUA130_assertion
dcterms:description
"[The fact that the MP19To3 did not traffic to the membrane, instead appearing to be trapped within a subcellular compartment within the cell sheds further light on the cause of the cataract and microphthalmia observed in the MP19To3 mutation, and further sheds information on the pathway of MP19 transport to the cell membrane.]. 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:12379840
;
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:NP331211.RA-itFtr2SOQUxwNl-IDi5R4zyeCya0iVzHJrI7qotwUA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:15+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" .
}