@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP470069.RADGdXwYqrGHGPXL6-tTjEziRyy1xptu_xj0l9x_l6xLg
> .
@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:NP470069.RADGdXwYqrGHGPXL6-tTjEziRyy1xptu_xj0l9x_l6xLg130_head
{
this:
np:hasAssertion
dgn-np:NP470069.RADGdXwYqrGHGPXL6-tTjEziRyy1xptu_xj0l9x_l6xLg130_assertion
;
np:hasProvenance
dgn-np:NP470069.RADGdXwYqrGHGPXL6-tTjEziRyy1xptu_xj0l9x_l6xLg130_provenance
;
np:hasPublicationInfo
dgn-np:NP470069.RADGdXwYqrGHGPXL6-tTjEziRyy1xptu_xj0l9x_l6xLg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP470069.RADGdXwYqrGHGPXL6-tTjEziRyy1xptu_xj0l9x_l6xLg130_assertion
a
np:Assertion
.
dgn-np:NP470069.RADGdXwYqrGHGPXL6-tTjEziRyy1xptu_xj0l9x_l6xLg130_provenance
a
np:Provenance
.
dgn-np:NP470069.RADGdXwYqrGHGPXL6-tTjEziRyy1xptu_xj0l9x_l6xLg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP470069.RADGdXwYqrGHGPXL6-tTjEziRyy1xptu_xj0l9x_l6xLg130_assertion
{
miriam-gene:3856
a
ncit:C16612
.
lld:C0023890
a
ncit:C7057
.
dgn-gda:DGN7aaf304ba9deb8bf0c2a6013b81d346b
sio:SIO_000628
miriam-gene:3856
,
lld:C0023890
;
a
sio:SIO_001121
.
}
dgn-np:NP470069.RADGdXwYqrGHGPXL6-tTjEziRyy1xptu_xj0l9x_l6xLg130_provenance
{
dgn-np:NP470069.RADGdXwYqrGHGPXL6-tTjEziRyy1xptu_xj0l9x_l6xLg130_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_literature
;
sio:SIO_000772
miriam-pubmed:12724528
;
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:NP470069.RADGdXwYqrGHGPXL6-tTjEziRyy1xptu_xj0l9x_l6xLg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:42+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: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" .
}