@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP912897.RAqLVqD_B212QUMaoNr7hY8okoMM9p0QCC7S7nfZFY--Y
> .
@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:NP912897.RAqLVqD_B212QUMaoNr7hY8okoMM9p0QCC7S7nfZFY--Y130_head
{
this:
np:hasAssertion
dgn-np:NP912897.RAqLVqD_B212QUMaoNr7hY8okoMM9p0QCC7S7nfZFY--Y130_assertion
;
np:hasProvenance
dgn-np:NP912897.RAqLVqD_B212QUMaoNr7hY8okoMM9p0QCC7S7nfZFY--Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP912897.RAqLVqD_B212QUMaoNr7hY8okoMM9p0QCC7S7nfZFY--Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP912897.RAqLVqD_B212QUMaoNr7hY8okoMM9p0QCC7S7nfZFY--Y130_assertion
a
np:Assertion
.
dgn-np:NP912897.RAqLVqD_B212QUMaoNr7hY8okoMM9p0QCC7S7nfZFY--Y130_provenance
a
np:Provenance
.
dgn-np:NP912897.RAqLVqD_B212QUMaoNr7hY8okoMM9p0QCC7S7nfZFY--Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP912897.RAqLVqD_B212QUMaoNr7hY8okoMM9p0QCC7S7nfZFY--Y130_assertion
{
miriam-gene:100859927
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGN453c87d7b0f7cfc2456e448c9820803e
sio:SIO_000628
miriam-gene:100859927
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP912897.RAqLVqD_B212QUMaoNr7hY8okoMM9p0QCC7S7nfZFY--Y130_provenance
{
dgn-np:NP912897.RAqLVqD_B212QUMaoNr7hY8okoMM9p0QCC7S7nfZFY--Y130_assertion
dcterms:description
"[The expression pattern of NAMLAA in the myeloid lineage suggests that the monoclonal antibody AAA4, recognizing NAMLAA, is useful for discrimination between AML in the monocyte lineage and in the granulocyte lineage.]. 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:9242559
;
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:NP912897.RAqLVqD_B212QUMaoNr7hY8okoMM9p0QCC7S7nfZFY--Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:20+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" .
}