@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP687344.RA1VHsFck-nUmhya92lUceHcPalmw-Go5tPBM1glnAM6s
> .
@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:NP687344.RA1VHsFck-nUmhya92lUceHcPalmw-Go5tPBM1glnAM6s130_head
{
this:
np:hasAssertion
dgn-np:NP687344.RA1VHsFck-nUmhya92lUceHcPalmw-Go5tPBM1glnAM6s130_assertion
;
np:hasProvenance
dgn-np:NP687344.RA1VHsFck-nUmhya92lUceHcPalmw-Go5tPBM1glnAM6s130_provenance
;
np:hasPublicationInfo
dgn-np:NP687344.RA1VHsFck-nUmhya92lUceHcPalmw-Go5tPBM1glnAM6s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP687344.RA1VHsFck-nUmhya92lUceHcPalmw-Go5tPBM1glnAM6s130_assertion
a
np:Assertion
.
dgn-np:NP687344.RA1VHsFck-nUmhya92lUceHcPalmw-Go5tPBM1glnAM6s130_provenance
a
np:Provenance
.
dgn-np:NP687344.RA1VHsFck-nUmhya92lUceHcPalmw-Go5tPBM1glnAM6s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP687344.RA1VHsFck-nUmhya92lUceHcPalmw-Go5tPBM1glnAM6s130_assertion
{
miriam-gene:6696
a
ncit:C16612
.
lld:C0028259
a
ncit:C7057
.
dgn-gda:DGN0ab2f069400e1fedca7949464bffedeb
sio:SIO_000628
miriam-gene:6696
,
lld:C0028259
;
a
sio:SIO_001121
.
}
dgn-np:NP687344.RA1VHsFck-nUmhya92lUceHcPalmw-Go5tPBM1glnAM6s130_provenance
{
dgn-np:NP687344.RA1VHsFck-nUmhya92lUceHcPalmw-Go5tPBM1glnAM6s130_assertion
dcterms:description
"[Osteoblastic cells derived from digital bone in two Apert patients with the S252W mutation showed more prominent alkaline phosphatase activity, osteocalcin and osteopontin mRNA expression, and mineralized nodule formation compared with the control osteoblastic cells derived from two independent non-syndromic polydactyly patients.]. 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:15310757
;
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:NP687344.RA1VHsFck-nUmhya92lUceHcPalmw-Go5tPBM1glnAM6s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:58+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" .
}