@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1303528.RAg8uOPyJyrSuVVkjGBgPsAm0tRsrIcQ81To2qQuBPX3I
> .
@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:NP1303528.RAg8uOPyJyrSuVVkjGBgPsAm0tRsrIcQ81To2qQuBPX3I130_head
{
this:
np:hasAssertion
dgn-np:NP1303528.RAg8uOPyJyrSuVVkjGBgPsAm0tRsrIcQ81To2qQuBPX3I130_assertion
;
np:hasProvenance
dgn-np:NP1303528.RAg8uOPyJyrSuVVkjGBgPsAm0tRsrIcQ81To2qQuBPX3I130_provenance
;
np:hasPublicationInfo
dgn-np:NP1303528.RAg8uOPyJyrSuVVkjGBgPsAm0tRsrIcQ81To2qQuBPX3I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1303528.RAg8uOPyJyrSuVVkjGBgPsAm0tRsrIcQ81To2qQuBPX3I130_assertion
a
np:Assertion
.
dgn-np:NP1303528.RAg8uOPyJyrSuVVkjGBgPsAm0tRsrIcQ81To2qQuBPX3I130_provenance
a
np:Provenance
.
dgn-np:NP1303528.RAg8uOPyJyrSuVVkjGBgPsAm0tRsrIcQ81To2qQuBPX3I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1303528.RAg8uOPyJyrSuVVkjGBgPsAm0tRsrIcQ81To2qQuBPX3I130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0018995
a
ncit:C7057
.
dgn-gda:DGNa3fd0e54c0fd93533a7d59b013fab955
sio:SIO_000628
miriam-gene:3077
,
lld:C0018995
;
a
sio:SIO_001121
.
}
dgn-np:NP1303528.RAg8uOPyJyrSuVVkjGBgPsAm0tRsrIcQ81To2qQuBPX3I130_provenance
{
dgn-np:NP1303528.RAg8uOPyJyrSuVVkjGBgPsAm0tRsrIcQ81To2qQuBPX3I130_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:NP1303528.RAg8uOPyJyrSuVVkjGBgPsAm0tRsrIcQ81To2qQuBPX3I130_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" .
}