@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP385874.RAO4fkmWbKn54IEHa8f-5iHhcH57z-YfrH3nlzNNv2v4Y
> .
@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:NP385874.RAO4fkmWbKn54IEHa8f-5iHhcH57z-YfrH3nlzNNv2v4Y130_head
{
this:
np:hasAssertion
dgn-np:NP385874.RAO4fkmWbKn54IEHa8f-5iHhcH57z-YfrH3nlzNNv2v4Y130_assertion
;
np:hasProvenance
dgn-np:NP385874.RAO4fkmWbKn54IEHa8f-5iHhcH57z-YfrH3nlzNNv2v4Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP385874.RAO4fkmWbKn54IEHa8f-5iHhcH57z-YfrH3nlzNNv2v4Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP385874.RAO4fkmWbKn54IEHa8f-5iHhcH57z-YfrH3nlzNNv2v4Y130_assertion
a
np:Assertion
.
dgn-np:NP385874.RAO4fkmWbKn54IEHa8f-5iHhcH57z-YfrH3nlzNNv2v4Y130_provenance
a
np:Provenance
.
dgn-np:NP385874.RAO4fkmWbKn54IEHa8f-5iHhcH57z-YfrH3nlzNNv2v4Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP385874.RAO4fkmWbKn54IEHa8f-5iHhcH57z-YfrH3nlzNNv2v4Y130_assertion
{
miriam-gene:3853
a
ncit:C16612
.
lld:C0265334
a
ncit:C7057
.
dgn-gda:DGN6f01887de29ed5d530165ffb221afd01
sio:SIO_000628
miriam-gene:3853
,
lld:C0265334
;
a
sio:SIO_001121
.
}
dgn-np:NP385874.RAO4fkmWbKn54IEHa8f-5iHhcH57z-YfrH3nlzNNv2v4Y130_provenance
{
dgn-np:NP385874.RAO4fkmWbKn54IEHa8f-5iHhcH57z-YfrH3nlzNNv2v4Y130_assertion
dcterms:description
"[have identified KRT6C mutations in patients with focal palmoplantar keratoderma (FPPK), but debate concerning overlapping phenotypes between FPPK and pachyonychia congenita (PC) will continue because only one family has nail involvement.]. 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:20081885
;
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:NP385874.RAO4fkmWbKn54IEHa8f-5iHhcH57z-YfrH3nlzNNv2v4Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:50+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" .
}