@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP165279.RAKiUAb6PLYGTuAkWNsTGkZ6NIFAW8wDpkC8Y7vzLb35E
> .
@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:NP165279.RAKiUAb6PLYGTuAkWNsTGkZ6NIFAW8wDpkC8Y7vzLb35E130_head
{
this:
np:hasAssertion
dgn-np:NP165279.RAKiUAb6PLYGTuAkWNsTGkZ6NIFAW8wDpkC8Y7vzLb35E130_assertion
;
np:hasProvenance
dgn-np:NP165279.RAKiUAb6PLYGTuAkWNsTGkZ6NIFAW8wDpkC8Y7vzLb35E130_provenance
;
np:hasPublicationInfo
dgn-np:NP165279.RAKiUAb6PLYGTuAkWNsTGkZ6NIFAW8wDpkC8Y7vzLb35E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP165279.RAKiUAb6PLYGTuAkWNsTGkZ6NIFAW8wDpkC8Y7vzLb35E130_assertion
a
np:Assertion
.
dgn-np:NP165279.RAKiUAb6PLYGTuAkWNsTGkZ6NIFAW8wDpkC8Y7vzLb35E130_provenance
a
np:Provenance
.
dgn-np:NP165279.RAKiUAb6PLYGTuAkWNsTGkZ6NIFAW8wDpkC8Y7vzLb35E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP165279.RAKiUAb6PLYGTuAkWNsTGkZ6NIFAW8wDpkC8Y7vzLb35E130_assertion
{
miriam-gene:4070
a
ncit:C16612
.
lld:C0010036
a
ncit:C7057
.
dgn-gda:DGN06c5b997ee3e052be1da7ea8b79430e4
sio:SIO_000628
miriam-gene:4070
,
lld:C0010036
;
a
sio:SIO_001121
.
}
dgn-np:NP165279.RAKiUAb6PLYGTuAkWNsTGkZ6NIFAW8wDpkC8Y7vzLb35E130_provenance
{
dgn-np:NP165279.RAKiUAb6PLYGTuAkWNsTGkZ6NIFAW8wDpkC8Y7vzLb35E130_assertion
dcterms:description
"[Although gelatinous corneal dystrophy has previously been mapped to chromosome 1p and seems to be associated with mutations in the M1S1 gene, molecular genetic studies have been limited to Japanese patients.]. 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:12107443
;
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:NP165279.RAKiUAb6PLYGTuAkWNsTGkZ6NIFAW8wDpkC8Y7vzLb35E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:29+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" .
}