@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP798285.RA2RBRSMyDSCwOLvhn9_DSf80N_I9cz7s8S7DnOTDzWok
> .
@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:NP798285.RA2RBRSMyDSCwOLvhn9_DSf80N_I9cz7s8S7DnOTDzWok130_head
{
this:
np:hasAssertion
dgn-np:NP798285.RA2RBRSMyDSCwOLvhn9_DSf80N_I9cz7s8S7DnOTDzWok130_assertion
;
np:hasProvenance
dgn-np:NP798285.RA2RBRSMyDSCwOLvhn9_DSf80N_I9cz7s8S7DnOTDzWok130_provenance
;
np:hasPublicationInfo
dgn-np:NP798285.RA2RBRSMyDSCwOLvhn9_DSf80N_I9cz7s8S7DnOTDzWok130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP798285.RA2RBRSMyDSCwOLvhn9_DSf80N_I9cz7s8S7DnOTDzWok130_assertion
a
np:Assertion
.
dgn-np:NP798285.RA2RBRSMyDSCwOLvhn9_DSf80N_I9cz7s8S7DnOTDzWok130_provenance
a
np:Provenance
.
dgn-np:NP798285.RA2RBRSMyDSCwOLvhn9_DSf80N_I9cz7s8S7DnOTDzWok130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP798285.RA2RBRSMyDSCwOLvhn9_DSf80N_I9cz7s8S7DnOTDzWok130_assertion
{
miriam-gene:4548
a
ncit:C16612
.
lld:C3495426
a
ncit:C7057
.
dgn-gda:DGN1b1e9eabf68d6725b4c1d1e22cf8268c
sio:SIO_000628
miriam-gene:4548
,
lld:C3495426
;
a
sio:SIO_001121
.
}
dgn-np:NP798285.RA2RBRSMyDSCwOLvhn9_DSf80N_I9cz7s8S7DnOTDzWok130_provenance
{
dgn-np:NP798285.RA2RBRSMyDSCwOLvhn9_DSf80N_I9cz7s8S7DnOTDzWok130_assertion
dcterms:description
"[Yet unidentified abnormalities of MS or of any of the enzymes participating in the synthesis of methylated vitamin B12 may play an important role in the phenotypic expression of moderate hyperhomocysteinemia.]. 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:10780318
;
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:NP798285.RA2RBRSMyDSCwOLvhn9_DSf80N_I9cz7s8S7DnOTDzWok130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:10+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" .
}