@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP129108.RAa7Rk7bRAGtJ2ZVOrWgsG1g7AUfKp2zpcjrYxmSeVCpw
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP129108.RAa7Rk7bRAGtJ2ZVOrWgsG1g7AUfKp2zpcjrYxmSeVCpw130_head
{
this:
np:hasAssertion
dgn-np:NP129108.RAa7Rk7bRAGtJ2ZVOrWgsG1g7AUfKp2zpcjrYxmSeVCpw130_assertion
;
np:hasProvenance
dgn-np:NP129108.RAa7Rk7bRAGtJ2ZVOrWgsG1g7AUfKp2zpcjrYxmSeVCpw130_provenance
;
np:hasPublicationInfo
dgn-np:NP129108.RAa7Rk7bRAGtJ2ZVOrWgsG1g7AUfKp2zpcjrYxmSeVCpw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP129108.RAa7Rk7bRAGtJ2ZVOrWgsG1g7AUfKp2zpcjrYxmSeVCpw130_assertion
a
np:Assertion
.
dgn-np:NP129108.RAa7Rk7bRAGtJ2ZVOrWgsG1g7AUfKp2zpcjrYxmSeVCpw130_provenance
a
np:Provenance
.
dgn-np:NP129108.RAa7Rk7bRAGtJ2ZVOrWgsG1g7AUfKp2zpcjrYxmSeVCpw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP129108.RAa7Rk7bRAGtJ2ZVOrWgsG1g7AUfKp2zpcjrYxmSeVCpw130_assertion
{
miriam-gene:5265
a
ncit:C16612
.
lld:C0524910
a
ncit:C7057
.
dgn-gda:DGN8fb914458d8c5a5033df8a8fa8b93565
sio:SIO_000628
miriam-gene:5265
,
lld:C0524910
;
a
sio:SIO_001122
.
}
dgn-np:NP129108.RAa7Rk7bRAGtJ2ZVOrWgsG1g7AUfKp2zpcjrYxmSeVCpw130_provenance
{
dgn-np:NP129108.RAa7Rk7bRAGtJ2ZVOrWgsG1g7AUfKp2zpcjrYxmSeVCpw130_assertion
dcterms:description
"[The presence of the relatively high frequency of A1AT S and HFE H63D allele carriers in Egyptian cases of HCV liver cirrhosis suggest the necessity to implement routine molecular analysis of these genes for detection of risk genotypes among affected famil]. 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:16802007
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP129108.RAa7Rk7bRAGtJ2ZVOrWgsG1g7AUfKp2zpcjrYxmSeVCpw130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:52+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}