@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP507441.RAXDMXftJFJzeG-qQvkNn2nDfaUiHEou_IOUzefhHkWqw
> .
@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:NP507441.RAXDMXftJFJzeG-qQvkNn2nDfaUiHEou_IOUzefhHkWqw130_head
{
this:
np:hasAssertion
dgn-np:NP507441.RAXDMXftJFJzeG-qQvkNn2nDfaUiHEou_IOUzefhHkWqw130_assertion
;
np:hasProvenance
dgn-np:NP507441.RAXDMXftJFJzeG-qQvkNn2nDfaUiHEou_IOUzefhHkWqw130_provenance
;
np:hasPublicationInfo
dgn-np:NP507441.RAXDMXftJFJzeG-qQvkNn2nDfaUiHEou_IOUzefhHkWqw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP507441.RAXDMXftJFJzeG-qQvkNn2nDfaUiHEou_IOUzefhHkWqw130_assertion
a
np:Assertion
.
dgn-np:NP507441.RAXDMXftJFJzeG-qQvkNn2nDfaUiHEou_IOUzefhHkWqw130_provenance
a
np:Provenance
.
dgn-np:NP507441.RAXDMXftJFJzeG-qQvkNn2nDfaUiHEou_IOUzefhHkWqw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP507441.RAXDMXftJFJzeG-qQvkNn2nDfaUiHEou_IOUzefhHkWqw130_assertion
{
miriam-gene:5621
a
ncit:C16612
.
lld:C0162534
a
ncit:C7057
.
dgn-gda:DGN6e5802ea7dee5ac2a4f864d7f9563bae
sio:SIO_000628
miriam-gene:5621
,
lld:C0162534
;
a
sio:SIO_001121
.
}
dgn-np:NP507441.RAXDMXftJFJzeG-qQvkNn2nDfaUiHEou_IOUzefhHkWqw130_provenance
{
dgn-np:NP507441.RAXDMXftJFJzeG-qQvkNn2nDfaUiHEou_IOUzefhHkWqw130_assertion
dcterms:description
"[The codon for the methionine at position 129 (M129) in the human prion protein provides an alternative initiation site for translation and renders individuals homozygous for M129 more susceptible to prion disease.]. 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:16081222
;
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:NP507441.RAXDMXftJFJzeG-qQvkNn2nDfaUiHEou_IOUzefhHkWqw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:35+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" .
}