@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP626322.RAu-PAfubqMtPuShgD1_Pq747QX6mgfhdmFSPP-lUXYT0
> .
@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:NP626322.RAu-PAfubqMtPuShgD1_Pq747QX6mgfhdmFSPP-lUXYT0130_head
{
this:
np:hasAssertion
dgn-np:NP626322.RAu-PAfubqMtPuShgD1_Pq747QX6mgfhdmFSPP-lUXYT0130_assertion
;
np:hasProvenance
dgn-np:NP626322.RAu-PAfubqMtPuShgD1_Pq747QX6mgfhdmFSPP-lUXYT0130_provenance
;
np:hasPublicationInfo
dgn-np:NP626322.RAu-PAfubqMtPuShgD1_Pq747QX6mgfhdmFSPP-lUXYT0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP626322.RAu-PAfubqMtPuShgD1_Pq747QX6mgfhdmFSPP-lUXYT0130_assertion
a
np:Assertion
.
dgn-np:NP626322.RAu-PAfubqMtPuShgD1_Pq747QX6mgfhdmFSPP-lUXYT0130_provenance
a
np:Provenance
.
dgn-np:NP626322.RAu-PAfubqMtPuShgD1_Pq747QX6mgfhdmFSPP-lUXYT0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP626322.RAu-PAfubqMtPuShgD1_Pq747QX6mgfhdmFSPP-lUXYT0130_assertion
{
miriam-gene:54998
a
ncit:C16612
.
lld:C0268328
a
ncit:C7057
.
dgn-gda:DGN860cb19ba6ca50c9377aa9ac6dbbba79
sio:SIO_000628
miriam-gene:54998
,
lld:C0268328
;
a
sio:SIO_001121
.
}
dgn-np:NP626322.RAu-PAfubqMtPuShgD1_Pq747QX6mgfhdmFSPP-lUXYT0130_provenance
{
dgn-np:NP626322.RAu-PAfubqMtPuShgD1_Pq747QX6mgfhdmFSPP-lUXYT0130_assertion
dcterms:description
"[The symptoms in this disease are similar to those seen in AIP, but ALAD porphyria can be differentiated from AIP by its autosomal recessive, rather than dominant, inheritance, by the lack of PBG overproduction, and by markedly decreased ALAD activity.]. 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:9516683
;
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:NP626322.RAu-PAfubqMtPuShgD1_Pq747QX6mgfhdmFSPP-lUXYT0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:18+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" .
}