@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1049939.RAhT-eWjwiEyjOsi5I_81O-YFl_kGkrlkJJ5Pg1uSl3rI
> .
@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:NP1049939.RAhT-eWjwiEyjOsi5I_81O-YFl_kGkrlkJJ5Pg1uSl3rI130_head
{
this:
np:hasAssertion
dgn-np:NP1049939.RAhT-eWjwiEyjOsi5I_81O-YFl_kGkrlkJJ5Pg1uSl3rI130_assertion
;
np:hasProvenance
dgn-np:NP1049939.RAhT-eWjwiEyjOsi5I_81O-YFl_kGkrlkJJ5Pg1uSl3rI130_provenance
;
np:hasPublicationInfo
dgn-np:NP1049939.RAhT-eWjwiEyjOsi5I_81O-YFl_kGkrlkJJ5Pg1uSl3rI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1049939.RAhT-eWjwiEyjOsi5I_81O-YFl_kGkrlkJJ5Pg1uSl3rI130_assertion
a
np:Assertion
.
dgn-np:NP1049939.RAhT-eWjwiEyjOsi5I_81O-YFl_kGkrlkJJ5Pg1uSl3rI130_provenance
a
np:Provenance
.
dgn-np:NP1049939.RAhT-eWjwiEyjOsi5I_81O-YFl_kGkrlkJJ5Pg1uSl3rI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1049939.RAhT-eWjwiEyjOsi5I_81O-YFl_kGkrlkJJ5Pg1uSl3rI130_assertion
{
miriam-gene:1410
a
ncit:C16612
.
lld:C0026848
a
ncit:C7057
.
dgn-gda:DGN801a7dc4c69e5222f949c89078863c65
sio:SIO_000628
miriam-gene:1410
,
lld:C0026848
;
a
sio:SIO_001121
.
}
dgn-np:NP1049939.RAhT-eWjwiEyjOsi5I_81O-YFl_kGkrlkJJ5Pg1uSl3rI130_provenance
{
dgn-np:NP1049939.RAhT-eWjwiEyjOsi5I_81O-YFl_kGkrlkJJ5Pg1uSl3rI130_assertion
dcterms:description
"[Multiple effects of HspB5 mutations are analyzed, and data are presented indicating that mutations of this protein are accompanied by development of different congenital diseases, such as cataract and different types of myopathies.]. 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:23379525
;
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:NP1049939.RAhT-eWjwiEyjOsi5I_81O-YFl_kGkrlkJJ5Pg1uSl3rI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:42+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" .
}