@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1334986.RALQSAI7vyHY9Ga036nBxED8u_JSTE4YjOjnomYJVv9Yw
> .
@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/
> .
dgn-np:NP1334986.RALQSAI7vyHY9Ga036nBxED8u_JSTE4YjOjnomYJVv9Yw130_head
{
this:
np:hasAssertion
dgn-np:NP1334986.RALQSAI7vyHY9Ga036nBxED8u_JSTE4YjOjnomYJVv9Yw130_assertion
;
np:hasProvenance
dgn-np:NP1334986.RALQSAI7vyHY9Ga036nBxED8u_JSTE4YjOjnomYJVv9Yw130_provenance
;
np:hasPublicationInfo
dgn-np:NP1334986.RALQSAI7vyHY9Ga036nBxED8u_JSTE4YjOjnomYJVv9Yw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1334986.RALQSAI7vyHY9Ga036nBxED8u_JSTE4YjOjnomYJVv9Yw130_assertion
a
np:Assertion
.
dgn-np:NP1334986.RALQSAI7vyHY9Ga036nBxED8u_JSTE4YjOjnomYJVv9Yw130_provenance
a
np:Provenance
.
dgn-np:NP1334986.RALQSAI7vyHY9Ga036nBxED8u_JSTE4YjOjnomYJVv9Yw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1334986.RALQSAI7vyHY9Ga036nBxED8u_JSTE4YjOjnomYJVv9Yw130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0282193
a
ncit:C7057
.
dgn-gda:DGN13fc249f06fd94223a73acca6ee8458f
sio:SIO_000628
miriam-gene:3077
,
lld:C0282193
;
a
sio:SIO_001121
.
}
dgn-np:NP1334986.RALQSAI7vyHY9Ga036nBxED8u_JSTE4YjOjnomYJVv9Yw130_provenance
{
dgn-np:NP1334986.RALQSAI7vyHY9Ga036nBxED8u_JSTE4YjOjnomYJVv9Yw130_assertion
dcterms:description
"[The patient was considered heterozygote for hemochromatosis on the basis of the autosomal recessive inheritance for hemochromatosis, the frequency of the hemochromatosis gene, and the laboratory parameters defining her iron overload.]. 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:8186659
;
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:NP1334986.RALQSAI7vyHY9Ga036nBxED8u_JSTE4YjOjnomYJVv9Yw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:51+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:disgenetv3.0rdf
;
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" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}