@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP573584.RAvhCCJwnVKfddf3Zzsoc8coSclixYPqeaDADzt6q5LFw
> .
@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:NP573584.RAvhCCJwnVKfddf3Zzsoc8coSclixYPqeaDADzt6q5LFw130_head
{
this:
np:hasAssertion
dgn-np:NP573584.RAvhCCJwnVKfddf3Zzsoc8coSclixYPqeaDADzt6q5LFw130_assertion
;
np:hasProvenance
dgn-np:NP573584.RAvhCCJwnVKfddf3Zzsoc8coSclixYPqeaDADzt6q5LFw130_provenance
;
np:hasPublicationInfo
dgn-np:NP573584.RAvhCCJwnVKfddf3Zzsoc8coSclixYPqeaDADzt6q5LFw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP573584.RAvhCCJwnVKfddf3Zzsoc8coSclixYPqeaDADzt6q5LFw130_assertion
a
np:Assertion
.
dgn-np:NP573584.RAvhCCJwnVKfddf3Zzsoc8coSclixYPqeaDADzt6q5LFw130_provenance
a
np:Provenance
.
dgn-np:NP573584.RAvhCCJwnVKfddf3Zzsoc8coSclixYPqeaDADzt6q5LFw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP573584.RAvhCCJwnVKfddf3Zzsoc8coSclixYPqeaDADzt6q5LFw130_assertion
{
miriam-gene:3630
a
ncit:C16612
.
lld:C0026848
a
ncit:C7057
.
dgn-gda:DGN6e34c1ff3c9131a7c39dc192eddb5205
sio:SIO_000628
miriam-gene:3630
,
lld:C0026848
;
a
sio:SIO_001121
.
}
dgn-np:NP573584.RAvhCCJwnVKfddf3Zzsoc8coSclixYPqeaDADzt6q5LFw130_provenance
{
dgn-np:NP573584.RAvhCCJwnVKfddf3Zzsoc8coSclixYPqeaDADzt6q5LFw130_assertion
dcterms:description
"[Insulin resistance manifested as impaired activation of glycogen synthase and thereby storage of glucose as glycogen in skeletal muscle is demonstrable early on in NIDDM relatives, suggesting that NIDDM could be an inherited muscle disease.]. 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:1485943
;
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:NP573584.RAvhCCJwnVKfddf3Zzsoc8coSclixYPqeaDADzt6q5LFw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:45+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" .
}