@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP242260.RA0txw-BnTGDQz4FEYwr1fGJlj7E5m9uPxScgLa2NyVqA
> .
@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:NP242260.RA0txw-BnTGDQz4FEYwr1fGJlj7E5m9uPxScgLa2NyVqA130_head
{
this:
np:hasAssertion
dgn-np:NP242260.RA0txw-BnTGDQz4FEYwr1fGJlj7E5m9uPxScgLa2NyVqA130_assertion
;
np:hasProvenance
dgn-np:NP242260.RA0txw-BnTGDQz4FEYwr1fGJlj7E5m9uPxScgLa2NyVqA130_provenance
;
np:hasPublicationInfo
dgn-np:NP242260.RA0txw-BnTGDQz4FEYwr1fGJlj7E5m9uPxScgLa2NyVqA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP242260.RA0txw-BnTGDQz4FEYwr1fGJlj7E5m9uPxScgLa2NyVqA130_assertion
a
np:Assertion
.
dgn-np:NP242260.RA0txw-BnTGDQz4FEYwr1fGJlj7E5m9uPxScgLa2NyVqA130_provenance
a
np:Provenance
.
dgn-np:NP242260.RA0txw-BnTGDQz4FEYwr1fGJlj7E5m9uPxScgLa2NyVqA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP242260.RA0txw-BnTGDQz4FEYwr1fGJlj7E5m9uPxScgLa2NyVqA130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGN54a65320bbbf5c56d757c174d148c43f
sio:SIO_000628
miriam-gene:3077
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP242260.RA0txw-BnTGDQz4FEYwr1fGJlj7E5m9uPxScgLa2NyVqA130_provenance
{
dgn-np:NP242260.RA0txw-BnTGDQz4FEYwr1fGJlj7E5m9uPxScgLa2NyVqA130_assertion
dcterms:description
"[DNA samples from 128 controls and 23 adult long-term survivors of acute myeloid leukemia (AML) treated at the Oulu University Hospital (Oulu, Finland) from 1987 to 2000 were examined for the presence of the C282Y and H63D mutations in HFE.]. 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:11399828
;
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:NP242260.RA0txw-BnTGDQz4FEYwr1fGJlj7E5m9uPxScgLa2NyVqA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:15+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" .
}