@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP612125.RAoiTRs3SA7ouKQ0xrQTq0vO5xbXxPW_i1CY7YE4_HJ0c
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP612125.RAoiTRs3SA7ouKQ0xrQTq0vO5xbXxPW_i1CY7YE4_HJ0c130_head
{
this:
np:hasAssertion
dgn-np:NP612125.RAoiTRs3SA7ouKQ0xrQTq0vO5xbXxPW_i1CY7YE4_HJ0c130_assertion
;
np:hasProvenance
dgn-np:NP612125.RAoiTRs3SA7ouKQ0xrQTq0vO5xbXxPW_i1CY7YE4_HJ0c130_provenance
;
np:hasPublicationInfo
dgn-np:NP612125.RAoiTRs3SA7ouKQ0xrQTq0vO5xbXxPW_i1CY7YE4_HJ0c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP612125.RAoiTRs3SA7ouKQ0xrQTq0vO5xbXxPW_i1CY7YE4_HJ0c130_assertion
a
np:Assertion
.
dgn-np:NP612125.RAoiTRs3SA7ouKQ0xrQTq0vO5xbXxPW_i1CY7YE4_HJ0c130_provenance
a
np:Provenance
.
dgn-np:NP612125.RAoiTRs3SA7ouKQ0xrQTq0vO5xbXxPW_i1CY7YE4_HJ0c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP612125.RAoiTRs3SA7ouKQ0xrQTq0vO5xbXxPW_i1CY7YE4_HJ0c130_assertion
{
miriam-gene:2328
a
ncit:C16612
.
lld:C0025517
a
ncit:C7057
.
dgn-gda:DGNba624541203591adf4908973b64fb0c3
sio:SIO_000628
miriam-gene:2328
,
lld:C0025517
;
a
sio:SIO_001122
.
}
dgn-np:NP612125.RAoiTRs3SA7ouKQ0xrQTq0vO5xbXxPW_i1CY7YE4_HJ0c130_provenance
{
dgn-np:NP612125.RAoiTRs3SA7ouKQ0xrQTq0vO5xbXxPW_i1CY7YE4_HJ0c130_assertion
dcterms:description
"[Numerous non-synonymous mutations in FMO3 have been identified in patients suffering from this metabolic disorder (e.g., N61S, M66I, P153L, and R492W), but the molecular mechanism(s) underlying the functional deficit attributed to these alleles has not been elucidated.]. 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:17531949
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP612125.RAoiTRs3SA7ouKQ0xrQTq0vO5xbXxPW_i1CY7YE4_HJ0c130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:23+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}