@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP228674.RAi7GVpAXfGYzk_1mBM5i4Fn6z5giQAIM2XYC8g3xhMho
> .
@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:NP228674.RAi7GVpAXfGYzk_1mBM5i4Fn6z5giQAIM2XYC8g3xhMho130_head
{
this:
np:hasAssertion
dgn-np:NP228674.RAi7GVpAXfGYzk_1mBM5i4Fn6z5giQAIM2XYC8g3xhMho130_assertion
;
np:hasProvenance
dgn-np:NP228674.RAi7GVpAXfGYzk_1mBM5i4Fn6z5giQAIM2XYC8g3xhMho130_provenance
;
np:hasPublicationInfo
dgn-np:NP228674.RAi7GVpAXfGYzk_1mBM5i4Fn6z5giQAIM2XYC8g3xhMho130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP228674.RAi7GVpAXfGYzk_1mBM5i4Fn6z5giQAIM2XYC8g3xhMho130_assertion
a
np:Assertion
.
dgn-np:NP228674.RAi7GVpAXfGYzk_1mBM5i4Fn6z5giQAIM2XYC8g3xhMho130_provenance
a
np:Provenance
.
dgn-np:NP228674.RAi7GVpAXfGYzk_1mBM5i4Fn6z5giQAIM2XYC8g3xhMho130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP228674.RAi7GVpAXfGYzk_1mBM5i4Fn6z5giQAIM2XYC8g3xhMho130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0524910
a
ncit:C7057
.
dgn-gda:DGNf4d9c21ee860497de31cce947987b200
sio:SIO_000628
miriam-gene:3077
,
lld:C0524910
;
a
sio:SIO_001121
.
}
dgn-np:NP228674.RAi7GVpAXfGYzk_1mBM5i4Fn6z5giQAIM2XYC8g3xhMho130_provenance
{
dgn-np:NP228674.RAi7GVpAXfGYzk_1mBM5i4Fn6z5giQAIM2XYC8g3xhMho130_assertion
dcterms:description
"[Although HFE mutations (especially the most frequent H63D mutation) are associated with increased iron loading, they are also associated with increased sustained virologic responses in US patients with advanced chronic hepatitis C.]. 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:17101320
;
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:NP228674.RAi7GVpAXfGYzk_1mBM5i4Fn6z5giQAIM2XYC8g3xhMho130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:08+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" .
}