@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP770954.RAA7dwQKVHepNJRwHKwK2wnnw35iPEC1PYg-nq2YfOs_k
> .
@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:NP770954.RAA7dwQKVHepNJRwHKwK2wnnw35iPEC1PYg-nq2YfOs_k130_head
{
this:
np:hasAssertion
dgn-np:NP770954.RAA7dwQKVHepNJRwHKwK2wnnw35iPEC1PYg-nq2YfOs_k130_assertion
;
np:hasProvenance
dgn-np:NP770954.RAA7dwQKVHepNJRwHKwK2wnnw35iPEC1PYg-nq2YfOs_k130_provenance
;
np:hasPublicationInfo
dgn-np:NP770954.RAA7dwQKVHepNJRwHKwK2wnnw35iPEC1PYg-nq2YfOs_k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP770954.RAA7dwQKVHepNJRwHKwK2wnnw35iPEC1PYg-nq2YfOs_k130_assertion
a
np:Assertion
.
dgn-np:NP770954.RAA7dwQKVHepNJRwHKwK2wnnw35iPEC1PYg-nq2YfOs_k130_provenance
a
np:Provenance
.
dgn-np:NP770954.RAA7dwQKVHepNJRwHKwK2wnnw35iPEC1PYg-nq2YfOs_k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP770954.RAA7dwQKVHepNJRwHKwK2wnnw35iPEC1PYg-nq2YfOs_k130_assertion
{
miriam-gene:2395
a
ncit:C16612
.
lld:C0878682
a
ncit:C7057
.
dgn-gda:DGN1939000bae8a85cda0de6d7880b5f5fe
sio:SIO_000628
miriam-gene:2395
,
lld:C0878682
;
a
sio:SIO_001121
.
}
dgn-np:NP770954.RAA7dwQKVHepNJRwHKwK2wnnw35iPEC1PYg-nq2YfOs_k130_provenance
{
dgn-np:NP770954.RAA7dwQKVHepNJRwHKwK2wnnw35iPEC1PYg-nq2YfOs_k130_assertion
dcterms:description
"[Many of these disorders are characterized by iron overload and include relatively common diseases such as hereditary hemochromatosis, rare abnormalities of plasma protein synthesis (atransferrinemia and aceruloplasminemia), and the neuromuscular disease Friedreich ataxia.]. 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:11419690
;
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:NP770954.RAA7dwQKVHepNJRwHKwK2wnnw35iPEC1PYg-nq2YfOs_k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:46+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" .
}