@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP757266.RABZ0GIs9gClbXACcrerpdpQlwxiwQzF-PBMDnzLYUI0g
> .
@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/v4.0.0/void/
> .
dgn-np:NP757266.RABZ0GIs9gClbXACcrerpdpQlwxiwQzF-PBMDnzLYUI0g130_head
{
this:
np:hasAssertion
dgn-np:NP757266.RABZ0GIs9gClbXACcrerpdpQlwxiwQzF-PBMDnzLYUI0g130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP757266.RABZ0GIs9gClbXACcrerpdpQlwxiwQzF-PBMDnzLYUI0g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP757266.RABZ0GIs9gClbXACcrerpdpQlwxiwQzF-PBMDnzLYUI0g130_assertion
a
np:Assertion
.
dgn-np:NP757266.RABZ0GIs9gClbXACcrerpdpQlwxiwQzF-PBMDnzLYUI0g130_provenance
a
np:Provenance
.
dgn-np:NP757266.RABZ0GIs9gClbXACcrerpdpQlwxiwQzF-PBMDnzLYUI0g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP757266.RABZ0GIs9gClbXACcrerpdpQlwxiwQzF-PBMDnzLYUI0g130_assertion
{
miriam-gene:2158
a
ncit:C16612
.
lld:C0008533
a
ncit:C7057
.
dgn-gda:DGNab5698ac25b4317840b377f5897113ac
sio:SIO_000628
miriam-gene:2158
,
lld:C0008533
;
a
sio:SIO_001121
.
}
dgn-np:NP757266.RABZ0GIs9gClbXACcrerpdpQlwxiwQzF-PBMDnzLYUI0g130_provenance
{
dgn-np:NP757266.RABZ0GIs9gClbXACcrerpdpQlwxiwQzF-PBMDnzLYUI0g130_assertion
dcterms:description
"[The complete amplification of all functional parts of the Factor IX gene in combination with these new techniques should enable us to detect the majority of mutations leading to haemophilia B.]. 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:1967542
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP757266.RABZ0GIs9gClbXACcrerpdpQlwxiwQzF-PBMDnzLYUI0g130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:28+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
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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
"v4.0.0.0" .
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pav:version
"v4.0.0" .
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