@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP968139.RABG2SXC73Z5gR89saGMrHud0EOvM73Rd8UoS8kjoffiM
> .
@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/v3.0.0/void/
> .
dgn-np:NP968139.RABG2SXC73Z5gR89saGMrHud0EOvM73Rd8UoS8kjoffiM130_head
{
this:
np:hasAssertion
dgn-np:NP968139.RABG2SXC73Z5gR89saGMrHud0EOvM73Rd8UoS8kjoffiM130_assertion
;
np:hasProvenance
dgn-np:NP968139.RABG2SXC73Z5gR89saGMrHud0EOvM73Rd8UoS8kjoffiM130_provenance
;
np:hasPublicationInfo
dgn-np:NP968139.RABG2SXC73Z5gR89saGMrHud0EOvM73Rd8UoS8kjoffiM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP968139.RABG2SXC73Z5gR89saGMrHud0EOvM73Rd8UoS8kjoffiM130_assertion
a
np:Assertion
.
dgn-np:NP968139.RABG2SXC73Z5gR89saGMrHud0EOvM73Rd8UoS8kjoffiM130_provenance
a
np:Provenance
.
dgn-np:NP968139.RABG2SXC73Z5gR89saGMrHud0EOvM73Rd8UoS8kjoffiM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP968139.RABG2SXC73Z5gR89saGMrHud0EOvM73Rd8UoS8kjoffiM130_assertion
{
miriam-gene:123811
a
ncit:C16612
.
lld:C0031485
a
ncit:C7057
.
dgn-gda:DGN614fa30a50e99dd4016797e6fc424921
sio:SIO_000628
miriam-gene:123811
,
lld:C0031485
;
a
sio:SIO_001121
.
}
dgn-np:NP968139.RABG2SXC73Z5gR89saGMrHud0EOvM73Rd8UoS8kjoffiM130_provenance
{
dgn-np:NP968139.RABG2SXC73Z5gR89saGMrHud0EOvM73Rd8UoS8kjoffiM130_assertion
dcterms:description
"[Massachusetts currently offers an optional expanded newborn screening programme that tests for 20 biochemical genetic disorders in addition to the mandated newborn screening tests, including phenylketonuria (PKU) and nine other biochemical genetic 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:16435173
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP968139.RABG2SXC73Z5gR89saGMrHud0EOvM73Rd8UoS8kjoffiM130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:31+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}