@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP88890.RAjrDoeRwbUM5_TD204haQhh8qGoCZOOdn2A0Syf4-jJM
> .
@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/v3.0.0/void/
> .
dgn-np:NP88890.RAjrDoeRwbUM5_TD204haQhh8qGoCZOOdn2A0Syf4-jJM130_head
{
this:
np:hasAssertion
dgn-np:NP88890.RAjrDoeRwbUM5_TD204haQhh8qGoCZOOdn2A0Syf4-jJM130_assertion
;
np:hasProvenance
dgn-np:NP88890.RAjrDoeRwbUM5_TD204haQhh8qGoCZOOdn2A0Syf4-jJM130_provenance
;
np:hasPublicationInfo
dgn-np:NP88890.RAjrDoeRwbUM5_TD204haQhh8qGoCZOOdn2A0Syf4-jJM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP88890.RAjrDoeRwbUM5_TD204haQhh8qGoCZOOdn2A0Syf4-jJM130_assertion
a
np:Assertion
.
dgn-np:NP88890.RAjrDoeRwbUM5_TD204haQhh8qGoCZOOdn2A0Syf4-jJM130_provenance
a
np:Provenance
.
dgn-np:NP88890.RAjrDoeRwbUM5_TD204haQhh8qGoCZOOdn2A0Syf4-jJM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP88890.RAjrDoeRwbUM5_TD204haQhh8qGoCZOOdn2A0Syf4-jJM130_assertion
{
miriam-gene:5265
a
ncit:C16612
.
lld:C0149521
a
ncit:C7057
.
dgn-gda:DGN74ee2250b76b894f443c7687eb1318e8
sio:SIO_000628
miriam-gene:5265
,
lld:C0149521
;
a
sio:SIO_001122
.
}
dgn-np:NP88890.RAjrDoeRwbUM5_TD204haQhh8qGoCZOOdn2A0Syf4-jJM130_provenance
{
dgn-np:NP88890.RAjrDoeRwbUM5_TD204haQhh8qGoCZOOdn2A0Syf4-jJM130_assertion
dcterms:description
"[The percentage of N29I mutations in ACP patients was higher than that reported in other studies, while the percentage of N34S and AAT mutations in ACP and idiopathic CP patients was similar.]. 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:19657220
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP88890.RAjrDoeRwbUM5_TD204haQhh8qGoCZOOdn2A0Syf4-jJM130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:29+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}