@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP510668.RA_U_8_d_NpVKGFJhf7HKG3VPymCTCDh89SkLfQHtdff8
> .
@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:NP510668.RA_U_8_d_NpVKGFJhf7HKG3VPymCTCDh89SkLfQHtdff8130_head
{
this:
np:hasAssertion
dgn-np:NP510668.RA_U_8_d_NpVKGFJhf7HKG3VPymCTCDh89SkLfQHtdff8130_assertion
;
np:hasProvenance
dgn-np:NP510668.RA_U_8_d_NpVKGFJhf7HKG3VPymCTCDh89SkLfQHtdff8130_provenance
;
np:hasPublicationInfo
dgn-np:NP510668.RA_U_8_d_NpVKGFJhf7HKG3VPymCTCDh89SkLfQHtdff8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP510668.RA_U_8_d_NpVKGFJhf7HKG3VPymCTCDh89SkLfQHtdff8130_assertion
a
np:Assertion
.
dgn-np:NP510668.RA_U_8_d_NpVKGFJhf7HKG3VPymCTCDh89SkLfQHtdff8130_provenance
a
np:Provenance
.
dgn-np:NP510668.RA_U_8_d_NpVKGFJhf7HKG3VPymCTCDh89SkLfQHtdff8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP510668.RA_U_8_d_NpVKGFJhf7HKG3VPymCTCDh89SkLfQHtdff8130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0151445
a
ncit:C7057
.
dgn-gda:DGN23a4c6cfc88ecb11fd9e6ff14140e070
sio:SIO_000628
miriam-gene:4524
,
lld:C0151445
;
a
sio:SIO_001121
.
}
dgn-np:NP510668.RA_U_8_d_NpVKGFJhf7HKG3VPymCTCDh89SkLfQHtdff8130_provenance
{
dgn-np:NP510668.RA_U_8_d_NpVKGFJhf7HKG3VPymCTCDh89SkLfQHtdff8130_assertion
dcterms:description
"[We measured Hcy, von Willebrand factor (vWF), folic acid, and vitamin B12 plasma levels and analyzed the frequencies of MTHFR mutations in 30 patients with SSc and 12 patients with primary Raynaud's phenomenon (RP); 29 healthy subjects served as controls.]. 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:11093443
;
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:NP510668.RA_U_8_d_NpVKGFJhf7HKG3VPymCTCDh89SkLfQHtdff8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:04+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" .
}