@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP43852.RAtjqxgh9c10y_xIcX5AC60wGPWmtCLU91zEug6h92b7Y
> .
@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 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:NP43852.RAtjqxgh9c10y_xIcX5AC60wGPWmtCLU91zEug6h92b7Y130_head
{
this:
np:hasAssertion
dgn-np:NP43852.RAtjqxgh9c10y_xIcX5AC60wGPWmtCLU91zEug6h92b7Y130_assertion
;
np:hasProvenance
dgn-np:NP43852.RAtjqxgh9c10y_xIcX5AC60wGPWmtCLU91zEug6h92b7Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP43852.RAtjqxgh9c10y_xIcX5AC60wGPWmtCLU91zEug6h92b7Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP43852.RAtjqxgh9c10y_xIcX5AC60wGPWmtCLU91zEug6h92b7Y130_assertion
a
np:Assertion
.
dgn-np:NP43852.RAtjqxgh9c10y_xIcX5AC60wGPWmtCLU91zEug6h92b7Y130_provenance
a
np:Provenance
.
dgn-np:NP43852.RAtjqxgh9c10y_xIcX5AC60wGPWmtCLU91zEug6h92b7Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP43852.RAtjqxgh9c10y_xIcX5AC60wGPWmtCLU91zEug6h92b7Y130_assertion
{
miriam-gene:2525
a
ncit:C16612
.
lld:C0028754
a
ncit:C7057
.
dgn-gda:DGN7bb2c5f5c5c251f913b994f543d761f2
sio:SIO_000628
miriam-gene:2525
,
lld:C0028754
;
a
sio:SIO_001122
.
}
dgn-np:NP43852.RAtjqxgh9c10y_xIcX5AC60wGPWmtCLU91zEug6h92b7Y130_provenance
{
dgn-np:NP43852.RAtjqxgh9c10y_xIcX5AC60wGPWmtCLU91zEug6h92b7Y130_assertion
dct:description
"[The frequency of the Le(a-b-) phenotype may vary substantially in different populations. Identification of this new genetic marker of obesity may, for example, contribute to the explanation of individual and ethnic differences in the prevalence of 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:15832169
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP43852.RAtjqxgh9c10y_xIcX5AC60wGPWmtCLU91zEug6h92b7Y130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:20+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}