@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1303529.RABTXMUka8hey6q8sga4CxQ5ij3CXF0zk1X05iCQwUdq0
> .
@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:NP1303529.RABTXMUka8hey6q8sga4CxQ5ij3CXF0zk1X05iCQwUdq0130_head
{
this:
np:hasAssertion
dgn-np:NP1303529.RABTXMUka8hey6q8sga4CxQ5ij3CXF0zk1X05iCQwUdq0130_assertion
;
np:hasProvenance
dgn-np:NP1303529.RABTXMUka8hey6q8sga4CxQ5ij3CXF0zk1X05iCQwUdq0130_provenance
;
np:hasPublicationInfo
dgn-np:NP1303529.RABTXMUka8hey6q8sga4CxQ5ij3CXF0zk1X05iCQwUdq0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1303529.RABTXMUka8hey6q8sga4CxQ5ij3CXF0zk1X05iCQwUdq0130_assertion
a
np:Assertion
.
dgn-np:NP1303529.RABTXMUka8hey6q8sga4CxQ5ij3CXF0zk1X05iCQwUdq0130_provenance
a
np:Provenance
.
dgn-np:NP1303529.RABTXMUka8hey6q8sga4CxQ5ij3CXF0zk1X05iCQwUdq0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1303529.RABTXMUka8hey6q8sga4CxQ5ij3CXF0zk1X05iCQwUdq0130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C2674218
a
ncit:C7057
.
dgn-gda:DGN22f61a63af011df205b5833867e4fe54
sio:SIO_000628
miriam-gene:3077
,
lld:C2674218
;
a
sio:SIO_001121
.
}
dgn-np:NP1303529.RABTXMUka8hey6q8sga4CxQ5ij3CXF0zk1X05iCQwUdq0130_provenance
{
dgn-np:NP1303529.RABTXMUka8hey6q8sga4CxQ5ij3CXF0zk1X05iCQwUdq0130_assertion
dcterms:description
"[HLA typing, which permits the detection of the gene for hemochromatosis, indicates that all family members with hereditary spherocytosis who have abnormal iron metabolism or significant iron overload are heterozygous for the hemochromatosis gene.]. 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:3777017
;
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:NP1303529.RABTXMUka8hey6q8sga4CxQ5ij3CXF0zk1X05iCQwUdq0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:37+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" .
}