@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP468621.RAS7cWqE4CnuWlHs919wg96ih3g1ydGDX-J0CLbkFtMYI
> .
@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:NP468621.RAS7cWqE4CnuWlHs919wg96ih3g1ydGDX-J0CLbkFtMYI130_head
{
this:
np:hasAssertion
dgn-np:NP468621.RAS7cWqE4CnuWlHs919wg96ih3g1ydGDX-J0CLbkFtMYI130_assertion
;
np:hasProvenance
dgn-np:NP468621.RAS7cWqE4CnuWlHs919wg96ih3g1ydGDX-J0CLbkFtMYI130_provenance
;
np:hasPublicationInfo
dgn-np:NP468621.RAS7cWqE4CnuWlHs919wg96ih3g1ydGDX-J0CLbkFtMYI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP468621.RAS7cWqE4CnuWlHs919wg96ih3g1ydGDX-J0CLbkFtMYI130_assertion
a
np:Assertion
.
dgn-np:NP468621.RAS7cWqE4CnuWlHs919wg96ih3g1ydGDX-J0CLbkFtMYI130_provenance
a
np:Provenance
.
dgn-np:NP468621.RAS7cWqE4CnuWlHs919wg96ih3g1ydGDX-J0CLbkFtMYI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP468621.RAS7cWqE4CnuWlHs919wg96ih3g1ydGDX-J0CLbkFtMYI130_assertion
{
miriam-gene:353
a
ncit:C16612
.
lld:C0023374
a
ncit:C7057
.
dgn-gda:DGNa124297847aa97c3937a7df402fe48a1
sio:SIO_000628
miriam-gene:353
,
lld:C0023374
;
a
sio:SIO_001121
.
}
dgn-np:NP468621.RAS7cWqE4CnuWlHs919wg96ih3g1ydGDX-J0CLbkFtMYI130_provenance
{
dgn-np:NP468621.RAS7cWqE4CnuWlHs919wg96ih3g1ydGDX-J0CLbkFtMYI130_assertion
dcterms:description
"[In contrast, some hair roots from carriers of HPRT deficiency contained two zones of activity with the same relative proportion of APRT and HPRT as hair roots of normal homozygotes, while others contained decreased amounts of HPRT activity.]. 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:7398108
;
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:NP468621.RAS7cWqE4CnuWlHs919wg96ih3g1ydGDX-J0CLbkFtMYI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:41+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" .
}