@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP3677.RAi7vm017oewFxz0V4_dqUuWWWrfOGr8WNnv3HUFgGQeM
> .
@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 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:NP3677.RAi7vm017oewFxz0V4_dqUuWWWrfOGr8WNnv3HUFgGQeM130_head
{
this:
np:hasAssertion
dgn-np:NP3677.RAi7vm017oewFxz0V4_dqUuWWWrfOGr8WNnv3HUFgGQeM130_assertion
;
np:hasProvenance
dgn-np:NP3677.RAi7vm017oewFxz0V4_dqUuWWWrfOGr8WNnv3HUFgGQeM130_provenance
;
np:hasPublicationInfo
dgn-np:NP3677.RAi7vm017oewFxz0V4_dqUuWWWrfOGr8WNnv3HUFgGQeM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP3677.RAi7vm017oewFxz0V4_dqUuWWWrfOGr8WNnv3HUFgGQeM130_assertion
a
np:Assertion
.
dgn-np:NP3677.RAi7vm017oewFxz0V4_dqUuWWWrfOGr8WNnv3HUFgGQeM130_provenance
a
np:Provenance
.
dgn-np:NP3677.RAi7vm017oewFxz0V4_dqUuWWWrfOGr8WNnv3HUFgGQeM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP3677.RAi7vm017oewFxz0V4_dqUuWWWrfOGr8WNnv3HUFgGQeM130_assertion
{
miriam-gene:3856
a
ncit:C16612
.
lld:C1861556
a
ncit:C7057
.
dgn-gda:DGNbf813029d1ddc5a324564445d0c3e7a1
sio:SIO_000628
miriam-gene:3856
,
lld:C1861556
;
a
sio:SIO_001122
.
}
dgn-np:NP3677.RAi7vm017oewFxz0V4_dqUuWWWrfOGr8WNnv3HUFgGQeM130_provenance
{
dgn-np:NP3677.RAi7vm017oewFxz0V4_dqUuWWWrfOGr8WNnv3HUFgGQeM130_assertion
dcterms:description
"[Keratin 8 and 18 (K8K18) mutations are found in patients with cryptogenic cirrhosis, but the role of keratin mutations in noncryptogenic cirrhosis and the incidence of keratin mutations in the general population are not known.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:12724528
;
prov:wasDerivedFrom
dgn-void:uniprot-20130724
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
dgn-void:uniprot-20130724
pav:importedOn
"2013-07-24"^^
xsd:date
.
}
dgn-np:NP3677.RAi7vm017oewFxz0V4_dqUuWWWrfOGr8WNnv3HUFgGQeM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:31:59+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" .
}