@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA
> .
@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:NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_head
{
this:
np:hasAssertion
dgn-np:NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_assertion
;
np:hasProvenance
dgn-np:NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_provenance
;
np:hasPublicationInfo
dgn-np:NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_assertion
a
np:Assertion
.
dgn-np:NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_provenance
a
np:Provenance
.
dgn-np:NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_assertion
{
miriam-gene:2328
a
ncit:C16612
.
lld:C0025517
a
ncit:C7057
.
dgn-gda:DGNffe3f418d0c103e75328baebb12750c2
sio:SIO_000628
miriam-gene:2328
,
lld:C0025517
;
a
sio:SIO_001121
.
}
dgn-np:NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_provenance
{
dgn-np:NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_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-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:NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:16+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" .
}