@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP601368.RAPnFetgZ58lqME24v8T_WpxclkfXb5kp7PxaPhzo92tg
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP601368.RAPnFetgZ58lqME24v8T_WpxclkfXb5kp7PxaPhzo92tg130_head
{
this:
np:hasAssertion
dgn-np:NP601368.RAPnFetgZ58lqME24v8T_WpxclkfXb5kp7PxaPhzo92tg130_assertion
;
np:hasProvenance
dgn-np:NP601368.RAPnFetgZ58lqME24v8T_WpxclkfXb5kp7PxaPhzo92tg130_provenance
;
np:hasPublicationInfo
dgn-np:NP601368.RAPnFetgZ58lqME24v8T_WpxclkfXb5kp7PxaPhzo92tg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP601368.RAPnFetgZ58lqME24v8T_WpxclkfXb5kp7PxaPhzo92tg130_assertion
a
np:Assertion
.
dgn-np:NP601368.RAPnFetgZ58lqME24v8T_WpxclkfXb5kp7PxaPhzo92tg130_provenance
a
np:Provenance
.
dgn-np:NP601368.RAPnFetgZ58lqME24v8T_WpxclkfXb5kp7PxaPhzo92tg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP601368.RAPnFetgZ58lqME24v8T_WpxclkfXb5kp7PxaPhzo92tg130_assertion
{
miriam-gene:4942
a
ncit:C16612
.
lld:C0266526
a
ncit:C7057
.
dgn-gda:DGN84a6f405ccaad68161f2ce0fbe070e1f
sio:SIO_000628
miriam-gene:4942
,
lld:C0266526
;
a
sio:SIO_001121
.
}
dgn-np:NP601368.RAPnFetgZ58lqME24v8T_WpxclkfXb5kp7PxaPhzo92tg130_provenance
{
dgn-np:NP601368.RAPnFetgZ58lqME24v8T_WpxclkfXb5kp7PxaPhzo92tg130_assertion
dcterms:description
"[These results suggest that one of the OAT-related sequences on the X chromosome may be in close proximity to the Norrie disease locus and represent the first report which indicates that the OAT cDNA may be useful for the identification of carrier status and/or prenatal diagnosis.]. 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:2568328
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP601368.RAPnFetgZ58lqME24v8T_WpxclkfXb5kp7PxaPhzo92tg130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:39+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}