@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP370895.RAh9iuSVQTRXQGiJMxuysJlyQyyVQj3rbJokEAFZe653Q
> .
@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:NP370895.RAh9iuSVQTRXQGiJMxuysJlyQyyVQj3rbJokEAFZe653Q130_head
{
this:
np:hasAssertion
dgn-np:NP370895.RAh9iuSVQTRXQGiJMxuysJlyQyyVQj3rbJokEAFZe653Q130_assertion
;
np:hasProvenance
dgn-np:NP370895.RAh9iuSVQTRXQGiJMxuysJlyQyyVQj3rbJokEAFZe653Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP370895.RAh9iuSVQTRXQGiJMxuysJlyQyyVQj3rbJokEAFZe653Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP370895.RAh9iuSVQTRXQGiJMxuysJlyQyyVQj3rbJokEAFZe653Q130_assertion
a
np:Assertion
.
dgn-np:NP370895.RAh9iuSVQTRXQGiJMxuysJlyQyyVQj3rbJokEAFZe653Q130_provenance
a
np:Provenance
.
dgn-np:NP370895.RAh9iuSVQTRXQGiJMxuysJlyQyyVQj3rbJokEAFZe653Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP370895.RAh9iuSVQTRXQGiJMxuysJlyQyyVQj3rbJokEAFZe653Q130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0018995
a
ncit:C7057
.
dgn-gda:DGN06d90a01cf0078704a466193e4ff83ef
sio:SIO_000628
miriam-gene:3077
,
lld:C0018995
;
a
sio:SIO_001122
.
}
dgn-np:NP370895.RAh9iuSVQTRXQGiJMxuysJlyQyyVQj3rbJokEAFZe653Q130_provenance
{
dgn-np:NP370895.RAh9iuSVQTRXQGiJMxuysJlyQyyVQj3rbJokEAFZe653Q130_assertion
dcterms:description
"[The HFE S65C mutation may lead to mild to moderate hepatic iron overload but neither clinically manifest haemochromatosis nor iron associated extensive liver fibrosis was encountered in any of the patients carrying this mutation.]. 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:12377814
;
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:NP370895.RAh9iuSVQTRXQGiJMxuysJlyQyyVQj3rbJokEAFZe653Q130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:33+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" .
}