@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP871232.RAhNd6q4hbr7ZCR7_cC9jWzaJlTT_-3cPPgHcbAQ3iKwo
> .
@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/v4.0.0/void/
> .
dgn-np:NP871232.RAhNd6q4hbr7ZCR7_cC9jWzaJlTT_-3cPPgHcbAQ3iKwo130_head
{
this:
np:hasAssertion
dgn-np:NP871232.RAhNd6q4hbr7ZCR7_cC9jWzaJlTT_-3cPPgHcbAQ3iKwo130_assertion
;
np:hasProvenance
dgn-np:NP871232.RAhNd6q4hbr7ZCR7_cC9jWzaJlTT_-3cPPgHcbAQ3iKwo130_provenance
;
np:hasPublicationInfo
dgn-np:NP871232.RAhNd6q4hbr7ZCR7_cC9jWzaJlTT_-3cPPgHcbAQ3iKwo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP871232.RAhNd6q4hbr7ZCR7_cC9jWzaJlTT_-3cPPgHcbAQ3iKwo130_assertion
a
np:Assertion
.
dgn-np:NP871232.RAhNd6q4hbr7ZCR7_cC9jWzaJlTT_-3cPPgHcbAQ3iKwo130_provenance
a
np:Provenance
.
dgn-np:NP871232.RAhNd6q4hbr7ZCR7_cC9jWzaJlTT_-3cPPgHcbAQ3iKwo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP871232.RAhNd6q4hbr7ZCR7_cC9jWzaJlTT_-3cPPgHcbAQ3iKwo130_assertion
{
miriam-gene:3952
a
ncit:C16612
.
lld:C0028754
a
ncit:C7057
.
dgn-gda:DGNeed60d0e7e23acbac2b3f963546840a3
sio:SIO_000628
miriam-gene:3952
,
lld:C0028754
;
a
sio:SIO_001121
.
}
dgn-np:NP871232.RAhNd6q4hbr7ZCR7_cC9jWzaJlTT_-3cPPgHcbAQ3iKwo130_provenance
{
dgn-np:NP871232.RAhNd6q4hbr7ZCR7_cC9jWzaJlTT_-3cPPgHcbAQ3iKwo130_assertion
dcterms:description
"[In conclusion, finding this new mutation in the LEPR beside our previous mutation in the LEP gene implies that monogenic obesity syndromes may be common in the Egyptian population owing to the high rates of consanguineous marriages.]. 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:21306929
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP871232.RAhNd6q4hbr7ZCR7_cC9jWzaJlTT_-3cPPgHcbAQ3iKwo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:19+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}