@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP892575.RA_ZEXNhh6mJJNTQdd5x4UvTR-veNJRO9fKGs5epkeJuo
> .
@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:NP892575.RA_ZEXNhh6mJJNTQdd5x4UvTR-veNJRO9fKGs5epkeJuo130_head
{
this:
np:hasAssertion
dgn-np:NP892575.RA_ZEXNhh6mJJNTQdd5x4UvTR-veNJRO9fKGs5epkeJuo130_assertion
;
np:hasProvenance
dgn-np:NP892575.RA_ZEXNhh6mJJNTQdd5x4UvTR-veNJRO9fKGs5epkeJuo130_provenance
;
np:hasPublicationInfo
dgn-np:NP892575.RA_ZEXNhh6mJJNTQdd5x4UvTR-veNJRO9fKGs5epkeJuo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP892575.RA_ZEXNhh6mJJNTQdd5x4UvTR-veNJRO9fKGs5epkeJuo130_assertion
a
np:Assertion
.
dgn-np:NP892575.RA_ZEXNhh6mJJNTQdd5x4UvTR-veNJRO9fKGs5epkeJuo130_provenance
a
np:Provenance
.
dgn-np:NP892575.RA_ZEXNhh6mJJNTQdd5x4UvTR-veNJRO9fKGs5epkeJuo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP892575.RA_ZEXNhh6mJJNTQdd5x4UvTR-veNJRO9fKGs5epkeJuo130_assertion
{
miriam-gene:448990
a
ncit:C16612
.
lld:C0030409
a
ncit:C7057
.
dgn-gda:DGNfbf090ec3d2464eb2e0fc3382d009547
sio:SIO_000628
miriam-gene:448990
,
lld:C0030409
;
a
sio:SIO_001121
.
}
dgn-np:NP892575.RA_ZEXNhh6mJJNTQdd5x4UvTR-veNJRO9fKGs5epkeJuo130_provenance
{
dgn-np:NP892575.RA_ZEXNhh6mJJNTQdd5x4UvTR-veNJRO9fKGs5epkeJuo130_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:NP892575.RA_ZEXNhh6mJJNTQdd5x4UvTR-veNJRO9fKGs5epkeJuo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:08+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" .
}