@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP829056.RAXXThPTUX3c3tEVr9klP8_p1EGJRvZeFljYotNMMRNuI
> .
@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:NP829056.RAXXThPTUX3c3tEVr9klP8_p1EGJRvZeFljYotNMMRNuI130_head
{
this:
np:hasAssertion
dgn-np:NP829056.RAXXThPTUX3c3tEVr9klP8_p1EGJRvZeFljYotNMMRNuI130_assertion
;
np:hasProvenance
dgn-np:NP829056.RAXXThPTUX3c3tEVr9klP8_p1EGJRvZeFljYotNMMRNuI130_provenance
;
np:hasPublicationInfo
dgn-np:NP829056.RAXXThPTUX3c3tEVr9klP8_p1EGJRvZeFljYotNMMRNuI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP829056.RAXXThPTUX3c3tEVr9klP8_p1EGJRvZeFljYotNMMRNuI130_assertion
a
np:Assertion
.
dgn-np:NP829056.RAXXThPTUX3c3tEVr9klP8_p1EGJRvZeFljYotNMMRNuI130_provenance
a
np:Provenance
.
dgn-np:NP829056.RAXXThPTUX3c3tEVr9klP8_p1EGJRvZeFljYotNMMRNuI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP829056.RAXXThPTUX3c3tEVr9klP8_p1EGJRvZeFljYotNMMRNuI130_assertion
{
miriam-gene:7126
a
ncit:C16612
.
lld:C0019880
a
ncit:C7057
.
dgn-gda:DGNc29eebb6cb41eaf3770660a30da62895
sio:SIO_000628
miriam-gene:7126
,
lld:C0019880
;
a
sio:SIO_001121
.
}
dgn-np:NP829056.RAXXThPTUX3c3tEVr9klP8_p1EGJRvZeFljYotNMMRNuI130_provenance
{
dgn-np:NP829056.RAXXThPTUX3c3tEVr9klP8_p1EGJRvZeFljYotNMMRNuI130_assertion
dcterms:description
"[Newborn screening for total homocysteine (tHcy) in blood may identify babies with vitamin B12 (B12) deficiency or homocystinuria, but data on the causes of increased tHcy in screening samples are sparse.]. 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:15319318
;
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:NP829056.RAXXThPTUX3c3tEVr9klP8_p1EGJRvZeFljYotNMMRNuI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:27+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" .
}