@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP795868.RAosqWtZafakTt_DnMQ2iJ1wskqg_SS8GFuhTHyl1lorg
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP795868.RAosqWtZafakTt_DnMQ2iJ1wskqg_SS8GFuhTHyl1lorg130_head
{
this:
np:hasAssertion
dgn-np:NP795868.RAosqWtZafakTt_DnMQ2iJ1wskqg_SS8GFuhTHyl1lorg130_assertion
;
np:hasProvenance
dgn-np:NP795868.RAosqWtZafakTt_DnMQ2iJ1wskqg_SS8GFuhTHyl1lorg130_provenance
;
np:hasPublicationInfo
dgn-np:NP795868.RAosqWtZafakTt_DnMQ2iJ1wskqg_SS8GFuhTHyl1lorg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP795868.RAosqWtZafakTt_DnMQ2iJ1wskqg_SS8GFuhTHyl1lorg130_assertion
a
np:Assertion
.
dgn-np:NP795868.RAosqWtZafakTt_DnMQ2iJ1wskqg_SS8GFuhTHyl1lorg130_provenance
a
np:Provenance
.
dgn-np:NP795868.RAosqWtZafakTt_DnMQ2iJ1wskqg_SS8GFuhTHyl1lorg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP795868.RAosqWtZafakTt_DnMQ2iJ1wskqg_SS8GFuhTHyl1lorg130_assertion
{
miriam-gene:8431
a
ncit:C16612
.
lld:C0011849
a
ncit:C7057
.
dgn-gda:DGN1c0b0ca19430e2f1850cf593cda43e23
sio:SIO_000628
miriam-gene:8431
,
lld:C0011849
;
a
sio:SIO_001121
.
}
dgn-np:NP795868.RAosqWtZafakTt_DnMQ2iJ1wskqg_SS8GFuhTHyl1lorg130_provenance
{
dgn-np:NP795868.RAosqWtZafakTt_DnMQ2iJ1wskqg_SS8GFuhTHyl1lorg130_assertion
dcterms:description
"[There was no association with corrected birth weight in 382 normal babies, but the only AA baby was 4,069 g. Our study suggests that genetic variation in SHP is unlikely to be common in the predisposition to diabetes, obesity, or increased birth weight in U.K. Caucasians.]. 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:12716764
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP795868.RAosqWtZafakTt_DnMQ2iJ1wskqg_SS8GFuhTHyl1lorg130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:41+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}