@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP805877.RAvXn512-jfmnzmksf2i3FAWp6xYuFveomGtzA7LgzMsY
> .
@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:NP805877.RAvXn512-jfmnzmksf2i3FAWp6xYuFveomGtzA7LgzMsY130_head
{
this:
np:hasAssertion
dgn-np:NP805877.RAvXn512-jfmnzmksf2i3FAWp6xYuFveomGtzA7LgzMsY130_assertion
;
np:hasProvenance
dgn-np:NP805877.RAvXn512-jfmnzmksf2i3FAWp6xYuFveomGtzA7LgzMsY130_provenance
;
np:hasPublicationInfo
dgn-np:NP805877.RAvXn512-jfmnzmksf2i3FAWp6xYuFveomGtzA7LgzMsY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP805877.RAvXn512-jfmnzmksf2i3FAWp6xYuFveomGtzA7LgzMsY130_assertion
a
np:Assertion
.
dgn-np:NP805877.RAvXn512-jfmnzmksf2i3FAWp6xYuFveomGtzA7LgzMsY130_provenance
a
np:Provenance
.
dgn-np:NP805877.RAvXn512-jfmnzmksf2i3FAWp6xYuFveomGtzA7LgzMsY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP805877.RAvXn512-jfmnzmksf2i3FAWp6xYuFveomGtzA7LgzMsY130_assertion
{
miriam-gene:6402
a
ncit:C16612
.
lld:C0011849
a
ncit:C7057
.
dgn-gda:DGN58cfa5fecbd6b30615acacfe74e68010
sio:SIO_000628
miriam-gene:6402
,
lld:C0011849
;
a
sio:SIO_001121
.
}
dgn-np:NP805877.RAvXn512-jfmnzmksf2i3FAWp6xYuFveomGtzA7LgzMsY130_provenance
{
dgn-np:NP805877.RAvXn512-jfmnzmksf2i3FAWp6xYuFveomGtzA7LgzMsY130_assertion
dcterms:description
"[The aim of our study was to evaluate the frequency of the L-selectin gene T668C mutation (from thymine to cytosine at position 668) resulted in F206L an amino acid substitution in patients with overt diabetes and their unaffected first degree relatives in comparison to the unselected control population.]. 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:11064106
;
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:NP805877.RAvXn512-jfmnzmksf2i3FAWp6xYuFveomGtzA7LgzMsY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:14+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" .
}