@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP164508.RAm-eA4Dr4OWI81CK8DZrB9dXmwYZZ-6Z9iKhzj9DnEok
> .
@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:NP164508.RAm-eA4Dr4OWI81CK8DZrB9dXmwYZZ-6Z9iKhzj9DnEok130_head
{
this:
np:hasAssertion
dgn-np:NP164508.RAm-eA4Dr4OWI81CK8DZrB9dXmwYZZ-6Z9iKhzj9DnEok130_assertion
;
np:hasProvenance
dgn-np:NP164508.RAm-eA4Dr4OWI81CK8DZrB9dXmwYZZ-6Z9iKhzj9DnEok130_provenance
;
np:hasPublicationInfo
dgn-np:NP164508.RAm-eA4Dr4OWI81CK8DZrB9dXmwYZZ-6Z9iKhzj9DnEok130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP164508.RAm-eA4Dr4OWI81CK8DZrB9dXmwYZZ-6Z9iKhzj9DnEok130_assertion
a
np:Assertion
.
dgn-np:NP164508.RAm-eA4Dr4OWI81CK8DZrB9dXmwYZZ-6Z9iKhzj9DnEok130_provenance
a
np:Provenance
.
dgn-np:NP164508.RAm-eA4Dr4OWI81CK8DZrB9dXmwYZZ-6Z9iKhzj9DnEok130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP164508.RAm-eA4Dr4OWI81CK8DZrB9dXmwYZZ-6Z9iKhzj9DnEok130_assertion
{
miriam-gene:3952
a
ncit:C16612
.
lld:C0028754
a
ncit:C7057
.
dgn-gda:DGNc7a0680387aecc750d9d6187080a80fb
sio:SIO_000628
miriam-gene:3952
,
lld:C0028754
;
a
sio:SIO_001121
.
}
dgn-np:NP164508.RAm-eA4Dr4OWI81CK8DZrB9dXmwYZZ-6Z9iKhzj9DnEok130_provenance
{
dgn-np:NP164508.RAm-eA4Dr4OWI81CK8DZrB9dXmwYZZ-6Z9iKhzj9DnEok130_assertion
dcterms:description
"[All familial effects were gone, and heritability estimates became virtually zero after adjustment of each of the OB traits and systolic blood pressure (SBP) in offspring for leptin values in parents.]. 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:15505633
;
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:NP164508.RAm-eA4Dr4OWI81CK8DZrB9dXmwYZZ-6Z9iKhzj9DnEok130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:29+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" .
}