@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP747098.RANfRsaBIfikLhVrSrufkpTplnjNgnn7LKUKXvDJxoYIw
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP747098.RANfRsaBIfikLhVrSrufkpTplnjNgnn7LKUKXvDJxoYIw130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP747098.RANfRsaBIfikLhVrSrufkpTplnjNgnn7LKUKXvDJxoYIw130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP747098.RANfRsaBIfikLhVrSrufkpTplnjNgnn7LKUKXvDJxoYIw130_assertion
a
np:Assertion
.
dgn-np:NP747098.RANfRsaBIfikLhVrSrufkpTplnjNgnn7LKUKXvDJxoYIw130_provenance
a
np:Provenance
.
dgn-np:NP747098.RANfRsaBIfikLhVrSrufkpTplnjNgnn7LKUKXvDJxoYIw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP747098.RANfRsaBIfikLhVrSrufkpTplnjNgnn7LKUKXvDJxoYIw130_assertion
{
miriam-gene:3953
a
ncit:C16612
.
lld:C0011849
a
ncit:C7057
.
dgn-gda:DGNc2042a72c3e2905275349f50b8a87299
sio:SIO_000628
miriam-gene:3953
,
lld:C0011849
;
a
sio:SIO_001121
.
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dgn-np:NP747098.RANfRsaBIfikLhVrSrufkpTplnjNgnn7LKUKXvDJxoYIw130_provenance
{
dgn-np:NP747098.RANfRsaBIfikLhVrSrufkpTplnjNgnn7LKUKXvDJxoYIw130_assertion
dcterms:description
"[As part of an effort to identify informative molecular markers for genetic analysis of human pedigrees segregating for obesity, we have developed a genetic map of human 1p in the region of the OB receptor (OBR), the gene that is defective in murine diabetes (Obrdb) and rat Zucker fatty (Obrfa) mutations located on mid-chromosome 4 and chromosome 5, respectively.]. 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:8743992
;
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:NP747098.RANfRsaBIfikLhVrSrufkpTplnjNgnn7LKUKXvDJxoYIw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:33+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
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dgn-void:disgenetrdf
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}