@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP735740.RArhDKeDhZQapetLAkZaa18C4Mh7E6chNpbm9ouzeNJns
> .
@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:NP735740.RArhDKeDhZQapetLAkZaa18C4Mh7E6chNpbm9ouzeNJns130_head
{
this:
np:hasAssertion
dgn-np:NP735740.RArhDKeDhZQapetLAkZaa18C4Mh7E6chNpbm9ouzeNJns130_assertion
;
np:hasProvenance
dgn-np:NP735740.RArhDKeDhZQapetLAkZaa18C4Mh7E6chNpbm9ouzeNJns130_provenance
;
np:hasPublicationInfo
dgn-np:NP735740.RArhDKeDhZQapetLAkZaa18C4Mh7E6chNpbm9ouzeNJns130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP735740.RArhDKeDhZQapetLAkZaa18C4Mh7E6chNpbm9ouzeNJns130_assertion
a
np:Assertion
.
dgn-np:NP735740.RArhDKeDhZQapetLAkZaa18C4Mh7E6chNpbm9ouzeNJns130_provenance
a
np:Provenance
.
dgn-np:NP735740.RArhDKeDhZQapetLAkZaa18C4Mh7E6chNpbm9ouzeNJns130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP735740.RArhDKeDhZQapetLAkZaa18C4Mh7E6chNpbm9ouzeNJns130_assertion
{
miriam-gene:25978
a
ncit:C16612
.
lld:C0240066
a
ncit:C7057
.
dgn-gda:DGN43e394d6cce8d2684e0a566e8435c81b
sio:SIO_000628
miriam-gene:25978
,
lld:C0240066
;
a
sio:SIO_001121
.
}
dgn-np:NP735740.RArhDKeDhZQapetLAkZaa18C4Mh7E6chNpbm9ouzeNJns130_provenance
{
dgn-np:NP735740.RArhDKeDhZQapetLAkZaa18C4Mh7E6chNpbm9ouzeNJns130_assertion
dcterms:description
"[HFE deficiency in intestinal crypt cells is thought to cause intestinal iron deficiency and greater expression of iron transporters such as SLC11A2 (also called DMT1, DCT1 and NRAMP2) and SLC11A3 (also called IREG1, ferroportin and MTP1; ref.]. 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:12704390
;
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:NP735740.RArhDKeDhZQapetLAkZaa18C4Mh7E6chNpbm9ouzeNJns130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:26+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" .
}