@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP249979.RAcLW6X3Rh9Jt9Gt8GE9E4xTvGd1r_eUa2xV4jHReIeb8
> .
@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:NP249979.RAcLW6X3Rh9Jt9Gt8GE9E4xTvGd1r_eUa2xV4jHReIeb8130_head
{
this:
np:hasAssertion
dgn-np:NP249979.RAcLW6X3Rh9Jt9Gt8GE9E4xTvGd1r_eUa2xV4jHReIeb8130_assertion
;
np:hasProvenance
dgn-np:NP249979.RAcLW6X3Rh9Jt9Gt8GE9E4xTvGd1r_eUa2xV4jHReIeb8130_provenance
;
np:hasPublicationInfo
dgn-np:NP249979.RAcLW6X3Rh9Jt9Gt8GE9E4xTvGd1r_eUa2xV4jHReIeb8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP249979.RAcLW6X3Rh9Jt9Gt8GE9E4xTvGd1r_eUa2xV4jHReIeb8130_assertion
a
np:Assertion
.
dgn-np:NP249979.RAcLW6X3Rh9Jt9Gt8GE9E4xTvGd1r_eUa2xV4jHReIeb8130_provenance
a
np:Provenance
.
dgn-np:NP249979.RAcLW6X3Rh9Jt9Gt8GE9E4xTvGd1r_eUa2xV4jHReIeb8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP249979.RAcLW6X3Rh9Jt9Gt8GE9E4xTvGd1r_eUa2xV4jHReIeb8130_assertion
{
miriam-gene:3643
a
ncit:C16612
.
lld:C0019247
a
ncit:C7057
.
dgn-gda:DGN973614892141c070939821e535d83a51
sio:SIO_000628
miriam-gene:3643
,
lld:C0019247
;
a
sio:SIO_001121
.
}
dgn-np:NP249979.RAcLW6X3Rh9Jt9Gt8GE9E4xTvGd1r_eUa2xV4jHReIeb8130_provenance
{
dgn-np:NP249979.RAcLW6X3Rh9Jt9Gt8GE9E4xTvGd1r_eUa2xV4jHReIeb8130_assertion
dcterms:description
"[We conclude that severity of insulin resistance in the proband may be explained by the genetic condition of compound heterozygote for IR mutations while severe insulin resistance in the mother raises the possibility that other genetic factors, like IRS-1 polymorphisms, may contribute to the phenotypic expression of IR mutations.]. 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:9175790
;
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:NP249979.RAcLW6X3Rh9Jt9Gt8GE9E4xTvGd1r_eUa2xV4jHReIeb8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:19+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" .
}