@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP594240.RAB7wWMRtYz5bDI1Ne6PxFhipSzlx5Z4Qt7jZu-paVGDQ
> .
@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:NP594240.RAB7wWMRtYz5bDI1Ne6PxFhipSzlx5Z4Qt7jZu-paVGDQ130_head
{
this:
np:hasAssertion
dgn-np:NP594240.RAB7wWMRtYz5bDI1Ne6PxFhipSzlx5Z4Qt7jZu-paVGDQ130_assertion
;
np:hasProvenance
dgn-np:NP594240.RAB7wWMRtYz5bDI1Ne6PxFhipSzlx5Z4Qt7jZu-paVGDQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP594240.RAB7wWMRtYz5bDI1Ne6PxFhipSzlx5Z4Qt7jZu-paVGDQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP594240.RAB7wWMRtYz5bDI1Ne6PxFhipSzlx5Z4Qt7jZu-paVGDQ130_assertion
a
np:Assertion
.
dgn-np:NP594240.RAB7wWMRtYz5bDI1Ne6PxFhipSzlx5Z4Qt7jZu-paVGDQ130_provenance
a
np:Provenance
.
dgn-np:NP594240.RAB7wWMRtYz5bDI1Ne6PxFhipSzlx5Z4Qt7jZu-paVGDQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP594240.RAB7wWMRtYz5bDI1Ne6PxFhipSzlx5Z4Qt7jZu-paVGDQ130_assertion
{
miriam-gene:9248
a
ncit:C16612
.
lld:C0028754
a
ncit:C7057
.
dgn-gda:DGN0b1d3eca31302c1967c20eb9808636b6
sio:SIO_000628
miriam-gene:9248
,
lld:C0028754
;
a
sio:SIO_001121
.
}
dgn-np:NP594240.RAB7wWMRtYz5bDI1Ne6PxFhipSzlx5Z4Qt7jZu-paVGDQ130_provenance
{
dgn-np:NP594240.RAB7wWMRtYz5bDI1Ne6PxFhipSzlx5Z4Qt7jZu-paVGDQ130_assertion
dcterms:description
"[We screened GPR50 for mutations in an obese cohort and identified an insertion of four amino acid residues (TTGH) at position 501, two common coding polymorphisms (T528A and V602I), and one noncoding polymorphism (C-16X2GPR50T).]. 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:16436372
;
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:NP594240.RAB7wWMRtYz5bDI1Ne6PxFhipSzlx5Z4Qt7jZu-paVGDQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:57+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" .
}