@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP532707.RA1Hmrv8-mP0kViJTOGeK8su3FT3Bk1Lo9014JAN8TlHU
> .
@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:NP532707.RA1Hmrv8-mP0kViJTOGeK8su3FT3Bk1Lo9014JAN8TlHU130_head
{
this:
np:hasAssertion
dgn-np:NP532707.RA1Hmrv8-mP0kViJTOGeK8su3FT3Bk1Lo9014JAN8TlHU130_assertion
;
np:hasProvenance
dgn-np:NP532707.RA1Hmrv8-mP0kViJTOGeK8su3FT3Bk1Lo9014JAN8TlHU130_provenance
;
np:hasPublicationInfo
dgn-np:NP532707.RA1Hmrv8-mP0kViJTOGeK8su3FT3Bk1Lo9014JAN8TlHU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP532707.RA1Hmrv8-mP0kViJTOGeK8su3FT3Bk1Lo9014JAN8TlHU130_assertion
a
np:Assertion
.
dgn-np:NP532707.RA1Hmrv8-mP0kViJTOGeK8su3FT3Bk1Lo9014JAN8TlHU130_provenance
a
np:Provenance
.
dgn-np:NP532707.RA1Hmrv8-mP0kViJTOGeK8su3FT3Bk1Lo9014JAN8TlHU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP532707.RA1Hmrv8-mP0kViJTOGeK8su3FT3Bk1Lo9014JAN8TlHU130_assertion
{
miriam-gene:4830
a
ncit:C16612
.
lld:C0019045
a
ncit:C7057
.
dgn-gda:DGN862b0639e1cdf413f852fc870be25cf9
sio:SIO_000628
miriam-gene:4830
,
lld:C0019045
;
a
sio:SIO_001121
.
}
dgn-np:NP532707.RA1Hmrv8-mP0kViJTOGeK8su3FT3Bk1Lo9014JAN8TlHU130_provenance
{
dgn-np:NP532707.RA1Hmrv8-mP0kViJTOGeK8su3FT3Bk1Lo9014JAN8TlHU130_assertion
dcterms:description
"[Together with coordinated follow-up systems in place, the Hemoglobinopathy Reference Laboratory has contributed to the success of the NBS program in the rapid identification and delivery of care to newborns with clinically significant Hb disorders.]. 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:21910601
;
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:NP532707.RA1Hmrv8-mP0kViJTOGeK8su3FT3Bk1Lo9014JAN8TlHU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:21+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" .
}