@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP652545.RAwUHDgsg7WfjLwF8RJdWL1n1URZVhkKZCedXBSqPm2_I
> .
@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/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@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/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP652545.RAwUHDgsg7WfjLwF8RJdWL1n1URZVhkKZCedXBSqPm2_I130_head
{
this:
np:hasAssertion
dgn-np:NP652545.RAwUHDgsg7WfjLwF8RJdWL1n1URZVhkKZCedXBSqPm2_I130_assertion
;
np:hasProvenance
dgn-np:NP652545.RAwUHDgsg7WfjLwF8RJdWL1n1URZVhkKZCedXBSqPm2_I130_provenance
;
np:hasPublicationInfo
dgn-np:NP652545.RAwUHDgsg7WfjLwF8RJdWL1n1URZVhkKZCedXBSqPm2_I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP652545.RAwUHDgsg7WfjLwF8RJdWL1n1URZVhkKZCedXBSqPm2_I130_assertion
a
np:Assertion
.
dgn-np:NP652545.RAwUHDgsg7WfjLwF8RJdWL1n1URZVhkKZCedXBSqPm2_I130_provenance
a
np:Provenance
.
dgn-np:NP652545.RAwUHDgsg7WfjLwF8RJdWL1n1URZVhkKZCedXBSqPm2_I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP652545.RAwUHDgsg7WfjLwF8RJdWL1n1URZVhkKZCedXBSqPm2_I130_assertion
{
miriam-gene:7431
a
ncit:C16612
.
lld:C0079298
a
ncit:C7057
.
dgn-gda:DGN5ae888075a10cbd26b7e089cf2f7f8e4
sio:SIO_000628
miriam-gene:7431
,
lld:C0079298
;
a
sio:SIO_001121
.
}
dgn-np:NP652545.RAwUHDgsg7WfjLwF8RJdWL1n1URZVhkKZCedXBSqPm2_I130_provenance
{
dgn-np:NP652545.RAwUHDgsg7WfjLwF8RJdWL1n1URZVhkKZCedXBSqPm2_I130_assertion
dcterms:description
"[Further, to explore possible correlations with function, the structural effects of the mutations in segment 2B of KRT5 and KRT14 and associated with EBS in our patients, as well as those reported previously, were modelled by molecular dynamics with the aid of the known crystal structure of the analogous segment of human vimentin.]. 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:20030639
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP652545.RAwUHDgsg7WfjLwF8RJdWL1n1URZVhkKZCedXBSqPm2_I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:33+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:disgenetrdf
;
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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}