@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP630685.RAuqvG5_iKgj9gfxBdWrMI9w_m0EJUT85AV4VSA_ZuC0o
> .
@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:NP630685.RAuqvG5_iKgj9gfxBdWrMI9w_m0EJUT85AV4VSA_ZuC0o130_head
{
this:
np:hasAssertion
dgn-np:NP630685.RAuqvG5_iKgj9gfxBdWrMI9w_m0EJUT85AV4VSA_ZuC0o130_assertion
;
np:hasProvenance
dgn-np:NP630685.RAuqvG5_iKgj9gfxBdWrMI9w_m0EJUT85AV4VSA_ZuC0o130_provenance
;
np:hasPublicationInfo
dgn-np:NP630685.RAuqvG5_iKgj9gfxBdWrMI9w_m0EJUT85AV4VSA_ZuC0o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP630685.RAuqvG5_iKgj9gfxBdWrMI9w_m0EJUT85AV4VSA_ZuC0o130_assertion
a
np:Assertion
.
dgn-np:NP630685.RAuqvG5_iKgj9gfxBdWrMI9w_m0EJUT85AV4VSA_ZuC0o130_provenance
a
np:Provenance
.
dgn-np:NP630685.RAuqvG5_iKgj9gfxBdWrMI9w_m0EJUT85AV4VSA_ZuC0o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP630685.RAuqvG5_iKgj9gfxBdWrMI9w_m0EJUT85AV4VSA_ZuC0o130_assertion
{
miriam-gene:477
a
ncit:C16612
.
lld:C1832884
a
ncit:C7057
.
dgn-gda:DGNe0ad0658fa63ed1a7f2350296b89a942
sio:SIO_000628
miriam-gene:477
,
lld:C1832884
;
a
sio:SIO_001121
.
}
dgn-np:NP630685.RAuqvG5_iKgj9gfxBdWrMI9w_m0EJUT85AV4VSA_ZuC0o130_provenance
{
dgn-np:NP630685.RAuqvG5_iKgj9gfxBdWrMI9w_m0EJUT85AV4VSA_ZuC0o130_assertion
dcterms:description
"[Besides the two novel mutations, the data here reported confirm the involvement of ATP1A2 gene in the sporadic form of HM, while the negative results on the other families tested for all genes known in HM strengthen the hypothesis of the existence of at least another locus involved in FHM.]. 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:17877748
;
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:NP630685.RAuqvG5_iKgj9gfxBdWrMI9w_m0EJUT85AV4VSA_ZuC0o130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:31+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" .
}