@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1252889.RA_ReJ-Kulmmafw2Xu2LyeLaRNPTZE_1zW09DbsQMU0zg
> .
@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/v4.0.0/void/
> .
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{
this:
np:hasAssertion
dgn-np:NP1252889.RA_ReJ-Kulmmafw2Xu2LyeLaRNPTZE_1zW09DbsQMU0zg130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP1252889.RA_ReJ-Kulmmafw2Xu2LyeLaRNPTZE_1zW09DbsQMU0zg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1252889.RA_ReJ-Kulmmafw2Xu2LyeLaRNPTZE_1zW09DbsQMU0zg130_assertion
a
np:Assertion
.
dgn-np:NP1252889.RA_ReJ-Kulmmafw2Xu2LyeLaRNPTZE_1zW09DbsQMU0zg130_provenance
a
np:Provenance
.
dgn-np:NP1252889.RA_ReJ-Kulmmafw2Xu2LyeLaRNPTZE_1zW09DbsQMU0zg130_publicationInfo
a
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.
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dgn-np:NP1252889.RA_ReJ-Kulmmafw2Xu2LyeLaRNPTZE_1zW09DbsQMU0zg130_assertion
{
miriam-gene:164656
a
ncit:C16612
.
lld:C0039730
a
ncit:C7057
.
dgn-gda:DGN0c35e68d58ad8b135b3d8f25c86c144f
sio:SIO_000628
miriam-gene:164656
,
lld:C0039730
;
a
sio:SIO_001122
.
}
dgn-np:NP1252889.RA_ReJ-Kulmmafw2Xu2LyeLaRNPTZE_1zW09DbsQMU0zg130_provenance
{
dgn-np:NP1252889.RA_ReJ-Kulmmafw2Xu2LyeLaRNPTZE_1zW09DbsQMU0zg130_assertion
dcterms:description
"[These results indicate that TMPRSS6 polymorphisms are more frequent in subjects with persistent IDA than in healthy controls, and in thalassemia carriers V736A variant may account for lower hemoglobin and MCV levels.]. 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:25557470
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1252889.RA_ReJ-Kulmmafw2Xu2LyeLaRNPTZE_1zW09DbsQMU0zg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:14+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
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;
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
"v4.0.0.0" .
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pav:version
"v4.0.0" .
}