@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP569486.RAxEpwf4W0ROZK20OLD3meGbMQN7c_GHxEzogFEph96Vs
> .
@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:NP569486.RAxEpwf4W0ROZK20OLD3meGbMQN7c_GHxEzogFEph96Vs130_head
{
this:
np:hasAssertion
dgn-np:NP569486.RAxEpwf4W0ROZK20OLD3meGbMQN7c_GHxEzogFEph96Vs130_assertion
;
np:hasProvenance
dgn-np:NP569486.RAxEpwf4W0ROZK20OLD3meGbMQN7c_GHxEzogFEph96Vs130_provenance
;
np:hasPublicationInfo
dgn-np:NP569486.RAxEpwf4W0ROZK20OLD3meGbMQN7c_GHxEzogFEph96Vs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP569486.RAxEpwf4W0ROZK20OLD3meGbMQN7c_GHxEzogFEph96Vs130_assertion
a
np:Assertion
.
dgn-np:NP569486.RAxEpwf4W0ROZK20OLD3meGbMQN7c_GHxEzogFEph96Vs130_provenance
a
np:Provenance
.
dgn-np:NP569486.RAxEpwf4W0ROZK20OLD3meGbMQN7c_GHxEzogFEph96Vs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP569486.RAxEpwf4W0ROZK20OLD3meGbMQN7c_GHxEzogFEph96Vs130_assertion
{
miriam-gene:2260
a
ncit:C16612
.
lld:C0239816
a
ncit:C7057
.
dgn-gda:DGN6dbc2e2a68ac02bb6d663b33ad4553a7
sio:SIO_000628
miriam-gene:2260
,
lld:C0239816
;
a
sio:SIO_001121
.
}
dgn-np:NP569486.RAxEpwf4W0ROZK20OLD3meGbMQN7c_GHxEzogFEph96Vs130_provenance
{
dgn-np:NP569486.RAxEpwf4W0ROZK20OLD3meGbMQN7c_GHxEzogFEph96Vs130_assertion
dcterms:description
"[The series of photographs range from the hands of an individual with FLG mutations but no history of eczema, to the hands of individuals with typical and atypical filaggrin hand eczema, and finally to the hands of an individual with FLG mutations and hand eczema caused by exposure to irritants and allergens.]. 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:22897780
;
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:NP569486.RAxEpwf4W0ROZK20OLD3meGbMQN7c_GHxEzogFEph96Vs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:43+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" .
}