@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP638248.RAxr545J8kTCYgLqIU1ia133HRGP6M92cVD9gicVKTXOY
> .
@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:NP638248.RAxr545J8kTCYgLqIU1ia133HRGP6M92cVD9gicVKTXOY130_head
{
this:
np:hasAssertion
dgn-np:NP638248.RAxr545J8kTCYgLqIU1ia133HRGP6M92cVD9gicVKTXOY130_assertion
;
np:hasProvenance
dgn-np:NP638248.RAxr545J8kTCYgLqIU1ia133HRGP6M92cVD9gicVKTXOY130_provenance
;
np:hasPublicationInfo
dgn-np:NP638248.RAxr545J8kTCYgLqIU1ia133HRGP6M92cVD9gicVKTXOY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP638248.RAxr545J8kTCYgLqIU1ia133HRGP6M92cVD9gicVKTXOY130_assertion
a
np:Assertion
.
dgn-np:NP638248.RAxr545J8kTCYgLqIU1ia133HRGP6M92cVD9gicVKTXOY130_provenance
a
np:Provenance
.
dgn-np:NP638248.RAxr545J8kTCYgLqIU1ia133HRGP6M92cVD9gicVKTXOY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP638248.RAxr545J8kTCYgLqIU1ia133HRGP6M92cVD9gicVKTXOY130_assertion
{
miriam-gene:338412
a
ncit:C16612
.
lld:C0030409
a
ncit:C7057
.
dgn-gda:DGN4e2b77c6b77c4257c8b9cb1258480ee9
sio:SIO_000628
miriam-gene:338412
,
lld:C0030409
;
a
sio:SIO_001121
.
}
dgn-np:NP638248.RAxr545J8kTCYgLqIU1ia133HRGP6M92cVD9gicVKTXOY130_provenance
{
dgn-np:NP638248.RAxr545J8kTCYgLqIU1ia133HRGP6M92cVD9gicVKTXOY130_assertion
dcterms:description
"[Paracoccidioidomycosis (PCM), the most important human systemic mycosis in Latin America, is known to be caused by at least four different phylogenetic lineages within the Paracoccidioides brasiliensis complex, including S1, PS2, PS3, and Pb01-like group.]. 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:22927496
;
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:NP638248.RAxr545J8kTCYgLqIU1ia133HRGP6M92cVD9gicVKTXOY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:25+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" .
}