@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP160172.RAU4NM98yd1mjz6FmDsawOj9iwRaEXn5FH_fw-i19CWrM
> .
@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:NP160172.RAU4NM98yd1mjz6FmDsawOj9iwRaEXn5FH_fw-i19CWrM130_assertion
;
np:hasProvenance
dgn-np:NP160172.RAU4NM98yd1mjz6FmDsawOj9iwRaEXn5FH_fw-i19CWrM130_provenance
;
np:hasPublicationInfo
dgn-np:NP160172.RAU4NM98yd1mjz6FmDsawOj9iwRaEXn5FH_fw-i19CWrM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP160172.RAU4NM98yd1mjz6FmDsawOj9iwRaEXn5FH_fw-i19CWrM130_assertion
a
np:Assertion
.
dgn-np:NP160172.RAU4NM98yd1mjz6FmDsawOj9iwRaEXn5FH_fw-i19CWrM130_provenance
a
np:Provenance
.
dgn-np:NP160172.RAU4NM98yd1mjz6FmDsawOj9iwRaEXn5FH_fw-i19CWrM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP160172.RAU4NM98yd1mjz6FmDsawOj9iwRaEXn5FH_fw-i19CWrM130_assertion
{
miriam-gene:2693
a
ncit:C16612
.
lld:C0028754
a
ncit:C7057
.
dgn-gda:DGNebf5ce9325578d827a24e0bb8900105b
sio:SIO_000628
miriam-gene:2693
,
lld:C0028754
;
a
sio:SIO_001121
.
}
dgn-np:NP160172.RAU4NM98yd1mjz6FmDsawOj9iwRaEXn5FH_fw-i19CWrM130_provenance
{
dgn-np:NP160172.RAU4NM98yd1mjz6FmDsawOj9iwRaEXn5FH_fw-i19CWrM130_assertion
dcterms:description
"[This linkage, together with significant transmission disequilibrium in families and replication of this association in an independent population, provides evidence that common SNPs and haplotypes within the GHSR region are involved in the pathogenesis of human obesity.]. 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:15616037
;
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:NP160172.RAU4NM98yd1mjz6FmDsawOj9iwRaEXn5FH_fw-i19CWrM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:26+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" .
}