@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP277210.RATjiOxdwgj0V4JaIMlx-5K305eXM9LnOE37YSzGuhDIQ
> .
@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:NP277210.RATjiOxdwgj0V4JaIMlx-5K305eXM9LnOE37YSzGuhDIQ130_head
{
this:
np:hasAssertion
dgn-np:NP277210.RATjiOxdwgj0V4JaIMlx-5K305eXM9LnOE37YSzGuhDIQ130_assertion
;
np:hasProvenance
dgn-np:NP277210.RATjiOxdwgj0V4JaIMlx-5K305eXM9LnOE37YSzGuhDIQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP277210.RATjiOxdwgj0V4JaIMlx-5K305eXM9LnOE37YSzGuhDIQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP277210.RATjiOxdwgj0V4JaIMlx-5K305eXM9LnOE37YSzGuhDIQ130_assertion
a
np:Assertion
.
dgn-np:NP277210.RATjiOxdwgj0V4JaIMlx-5K305eXM9LnOE37YSzGuhDIQ130_provenance
a
np:Provenance
.
dgn-np:NP277210.RATjiOxdwgj0V4JaIMlx-5K305eXM9LnOE37YSzGuhDIQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP277210.RATjiOxdwgj0V4JaIMlx-5K305eXM9LnOE37YSzGuhDIQ130_assertion
{
miriam-gene:773
a
ncit:C16612
.
lld:C1832903
a
ncit:C7057
.
dgn-gda:DGNeb037cd3960272c8b7c2ae614f89f008
sio:SIO_000628
miriam-gene:773
,
lld:C1832903
;
a
sio:SIO_001121
.
}
dgn-np:NP277210.RATjiOxdwgj0V4JaIMlx-5K305eXM9LnOE37YSzGuhDIQ130_provenance
{
dgn-np:NP277210.RATjiOxdwgj0V4JaIMlx-5K305eXM9LnOE37YSzGuhDIQ130_assertion
dcterms:description
"[Only very few DNA variants were identified in 100 SHM patients, and regardless of whether the identified variants are causal the CACNA1A and ATP1A2 genes are not major genes in SHM.]. 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:18513263
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP277210.RATjiOxdwgj0V4JaIMlx-5K305eXM9LnOE37YSzGuhDIQ130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:40:18+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" .
}