@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP924972.RATXWeIizLfzVfxPDgljpP_UdElY_MFmYK5yLWgb1q9mU
> .
@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:NP924972.RATXWeIizLfzVfxPDgljpP_UdElY_MFmYK5yLWgb1q9mU130_head
{
this:
np:hasAssertion
dgn-np:NP924972.RATXWeIizLfzVfxPDgljpP_UdElY_MFmYK5yLWgb1q9mU130_assertion
;
np:hasProvenance
dgn-np:NP924972.RATXWeIizLfzVfxPDgljpP_UdElY_MFmYK5yLWgb1q9mU130_provenance
;
np:hasPublicationInfo
dgn-np:NP924972.RATXWeIizLfzVfxPDgljpP_UdElY_MFmYK5yLWgb1q9mU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP924972.RATXWeIizLfzVfxPDgljpP_UdElY_MFmYK5yLWgb1q9mU130_assertion
a
np:Assertion
.
dgn-np:NP924972.RATXWeIizLfzVfxPDgljpP_UdElY_MFmYK5yLWgb1q9mU130_provenance
a
np:Provenance
.
dgn-np:NP924972.RATXWeIizLfzVfxPDgljpP_UdElY_MFmYK5yLWgb1q9mU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP924972.RATXWeIizLfzVfxPDgljpP_UdElY_MFmYK5yLWgb1q9mU130_assertion
{
miriam-gene:2592
a
ncit:C16612
.
lld:C0025322
a
ncit:C7057
.
dgn-gda:DGN283df1e479a9b640059a00bf50c1b4eb
sio:SIO_000628
miriam-gene:2592
,
lld:C0025322
;
a
sio:SIO_001121
.
}
dgn-np:NP924972.RATXWeIizLfzVfxPDgljpP_UdElY_MFmYK5yLWgb1q9mU130_provenance
{
dgn-np:NP924972.RATXWeIizLfzVfxPDgljpP_UdElY_MFmYK5yLWgb1q9mU130_assertion
dcterms:description
"[These data support the hypothesis that there is no significant association between GALT mutations and ovarian failure, and hence the present authors conclude that there is no relationship between ovarian failure and GALT polymorphisms in Indian women.]. 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:16274605
;
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:NP924972.RATXWeIizLfzVfxPDgljpP_UdElY_MFmYK5yLWgb1q9mU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:27+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" .
}