@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP640597.RA5PH2hT2B7XaM4ELGuufL70R23VUPqvvoO-VjzWrPkWE
> .
@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:NP640597.RA5PH2hT2B7XaM4ELGuufL70R23VUPqvvoO-VjzWrPkWE130_head
{
this:
np:hasAssertion
dgn-np:NP640597.RA5PH2hT2B7XaM4ELGuufL70R23VUPqvvoO-VjzWrPkWE130_assertion
;
np:hasProvenance
dgn-np:NP640597.RA5PH2hT2B7XaM4ELGuufL70R23VUPqvvoO-VjzWrPkWE130_provenance
;
np:hasPublicationInfo
dgn-np:NP640597.RA5PH2hT2B7XaM4ELGuufL70R23VUPqvvoO-VjzWrPkWE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP640597.RA5PH2hT2B7XaM4ELGuufL70R23VUPqvvoO-VjzWrPkWE130_assertion
a
np:Assertion
.
dgn-np:NP640597.RA5PH2hT2B7XaM4ELGuufL70R23VUPqvvoO-VjzWrPkWE130_provenance
a
np:Provenance
.
dgn-np:NP640597.RA5PH2hT2B7XaM4ELGuufL70R23VUPqvvoO-VjzWrPkWE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP640597.RA5PH2hT2B7XaM4ELGuufL70R23VUPqvvoO-VjzWrPkWE130_assertion
{
miriam-gene:445341
a
ncit:C16612
.
lld:C0020630
a
ncit:C7057
.
dgn-gda:DGN258c7f00329f137fbb16b1519a893c60
sio:SIO_000628
miriam-gene:445341
,
lld:C0020630
;
a
sio:SIO_001121
.
}
dgn-np:NP640597.RA5PH2hT2B7XaM4ELGuufL70R23VUPqvvoO-VjzWrPkWE130_provenance
{
dgn-np:NP640597.RA5PH2hT2B7XaM4ELGuufL70R23VUPqvvoO-VjzWrPkWE130_assertion
dcterms:description
"[Hypophosphatasia (HPP) is an inherited disorder characterised by defective bone and tooth mineralisation and deficient serum and bone alkaline phosphatase activity, and it results from mutations in alkaline phosphatase (ALPL) encoding tissue-nonspecific alkaline phosphatase (TNAP).]. 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:20828673
;
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:NP640597.RA5PH2hT2B7XaM4ELGuufL70R23VUPqvvoO-VjzWrPkWE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:26+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" .
}