@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP798592.RAiNeNLGnyiuPuadgD6e7eoWFj55PJxjijjHnjKchxXX0
> .
@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:NP798592.RAiNeNLGnyiuPuadgD6e7eoWFj55PJxjijjHnjKchxXX0130_head
{
this:
np:hasAssertion
dgn-np:NP798592.RAiNeNLGnyiuPuadgD6e7eoWFj55PJxjijjHnjKchxXX0130_assertion
;
np:hasProvenance
dgn-np:NP798592.RAiNeNLGnyiuPuadgD6e7eoWFj55PJxjijjHnjKchxXX0130_provenance
;
np:hasPublicationInfo
dgn-np:NP798592.RAiNeNLGnyiuPuadgD6e7eoWFj55PJxjijjHnjKchxXX0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP798592.RAiNeNLGnyiuPuadgD6e7eoWFj55PJxjijjHnjKchxXX0130_assertion
a
np:Assertion
.
dgn-np:NP798592.RAiNeNLGnyiuPuadgD6e7eoWFj55PJxjijjHnjKchxXX0130_provenance
a
np:Provenance
.
dgn-np:NP798592.RAiNeNLGnyiuPuadgD6e7eoWFj55PJxjijjHnjKchxXX0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP798592.RAiNeNLGnyiuPuadgD6e7eoWFj55PJxjijjHnjKchxXX0130_assertion
{
miriam-gene:34
a
ncit:C16612
.
lld:C0268635
a
ncit:C7057
.
dgn-gda:DGN4191b27814f96d3233ce510499ccfd7a
sio:SIO_000628
miriam-gene:34
,
lld:C0268635
;
a
sio:SIO_001121
.
}
dgn-np:NP798592.RAiNeNLGnyiuPuadgD6e7eoWFj55PJxjijjHnjKchxXX0130_provenance
{
dgn-np:NP798592.RAiNeNLGnyiuPuadgD6e7eoWFj55PJxjijjHnjKchxXX0130_assertion
dcterms:description
"[Currently available information from screening studies on the frequency of detection of MCADD in newborns, as well as the frequency of homozygotes for the common mutation in the ACADM gene, is summarized.]. 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:16617240
;
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:NP798592.RAiNeNLGnyiuPuadgD6e7eoWFj55PJxjijjHnjKchxXX0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:10+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" .
}