@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP343729.RAMThKZhlZV61qoLenNufM9DmjPSRjTZm6jJTlz9_8ifk
> .
@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:NP343729.RAMThKZhlZV61qoLenNufM9DmjPSRjTZm6jJTlz9_8ifk130_head
{
this:
np:hasAssertion
dgn-np:NP343729.RAMThKZhlZV61qoLenNufM9DmjPSRjTZm6jJTlz9_8ifk130_assertion
;
np:hasProvenance
dgn-np:NP343729.RAMThKZhlZV61qoLenNufM9DmjPSRjTZm6jJTlz9_8ifk130_provenance
;
np:hasPublicationInfo
dgn-np:NP343729.RAMThKZhlZV61qoLenNufM9DmjPSRjTZm6jJTlz9_8ifk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP343729.RAMThKZhlZV61qoLenNufM9DmjPSRjTZm6jJTlz9_8ifk130_assertion
a
np:Assertion
.
dgn-np:NP343729.RAMThKZhlZV61qoLenNufM9DmjPSRjTZm6jJTlz9_8ifk130_provenance
a
np:Provenance
.
dgn-np:NP343729.RAMThKZhlZV61qoLenNufM9DmjPSRjTZm6jJTlz9_8ifk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP343729.RAMThKZhlZV61qoLenNufM9DmjPSRjTZm6jJTlz9_8ifk130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0524851
a
ncit:C7057
.
dgn-gda:DGN33334aa07bbc2aa6559ed1d48f8bde08
sio:SIO_000628
miriam-gene:3077
,
lld:C0524851
;
a
sio:SIO_001121
.
}
dgn-np:NP343729.RAMThKZhlZV61qoLenNufM9DmjPSRjTZm6jJTlz9_8ifk130_provenance
{
dgn-np:NP343729.RAMThKZhlZV61qoLenNufM9DmjPSRjTZm6jJTlz9_8ifk130_assertion
dcterms:description
"[Because of the increasing evidence that H63D HFE polymorphism appears in higher frequency in neurodegenerative diseases, we evaluated the neurological consequences of H63D HFE in vivo using mice that carry H67D HFE (homologous to human H63D).]. 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:23429074
;
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:NP343729.RAMThKZhlZV61qoLenNufM9DmjPSRjTZm6jJTlz9_8ifk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:22+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" .
}