@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP481416.RAXN52Pt4zfLrKx57YE6N36OrmkV66T4bjZBPMGjKkJ4Y
> .
@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:NP481416.RAXN52Pt4zfLrKx57YE6N36OrmkV66T4bjZBPMGjKkJ4Y130_head
{
this:
np:hasAssertion
dgn-np:NP481416.RAXN52Pt4zfLrKx57YE6N36OrmkV66T4bjZBPMGjKkJ4Y130_assertion
;
np:hasProvenance
dgn-np:NP481416.RAXN52Pt4zfLrKx57YE6N36OrmkV66T4bjZBPMGjKkJ4Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP481416.RAXN52Pt4zfLrKx57YE6N36OrmkV66T4bjZBPMGjKkJ4Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP481416.RAXN52Pt4zfLrKx57YE6N36OrmkV66T4bjZBPMGjKkJ4Y130_assertion
a
np:Assertion
.
dgn-np:NP481416.RAXN52Pt4zfLrKx57YE6N36OrmkV66T4bjZBPMGjKkJ4Y130_provenance
a
np:Provenance
.
dgn-np:NP481416.RAXN52Pt4zfLrKx57YE6N36OrmkV66T4bjZBPMGjKkJ4Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP481416.RAXN52Pt4zfLrKx57YE6N36OrmkV66T4bjZBPMGjKkJ4Y130_assertion
{
miriam-gene:885
a
ncit:C16612
.
lld:C0011849
a
ncit:C7057
.
dgn-gda:DGN66bd800cf1844fff4b987b3e61a1a8f1
sio:SIO_000628
miriam-gene:885
,
lld:C0011849
;
a
sio:SIO_001121
.
}
dgn-np:NP481416.RAXN52Pt4zfLrKx57YE6N36OrmkV66T4bjZBPMGjKkJ4Y130_provenance
{
dgn-np:NP481416.RAXN52Pt4zfLrKx57YE6N36OrmkV66T4bjZBPMGjKkJ4Y130_assertion
dcterms:description
"[Although CCK-1R polymorphisms with amino acid changes such as 21Gly to Arg, 71 Arg to Gly, and 364 Val to Ile were discovered in subjects with obesity and diabetes mellitus, these changes occur sporadically.]. 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:17584142
;
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:NP481416.RAXN52Pt4zfLrKx57YE6N36OrmkV66T4bjZBPMGjKkJ4Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:48+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" .
}