@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP50715.RAP4cQVdpRxmdV8Gcv6AU5xpSVkNPgLN2LmzeeMoTQlBQ
> .
@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:NP50715.RAP4cQVdpRxmdV8Gcv6AU5xpSVkNPgLN2LmzeeMoTQlBQ130_head
{
this:
np:hasAssertion
dgn-np:NP50715.RAP4cQVdpRxmdV8Gcv6AU5xpSVkNPgLN2LmzeeMoTQlBQ130_assertion
;
np:hasProvenance
dgn-np:NP50715.RAP4cQVdpRxmdV8Gcv6AU5xpSVkNPgLN2LmzeeMoTQlBQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP50715.RAP4cQVdpRxmdV8Gcv6AU5xpSVkNPgLN2LmzeeMoTQlBQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP50715.RAP4cQVdpRxmdV8Gcv6AU5xpSVkNPgLN2LmzeeMoTQlBQ130_assertion
a
np:Assertion
.
dgn-np:NP50715.RAP4cQVdpRxmdV8Gcv6AU5xpSVkNPgLN2LmzeeMoTQlBQ130_provenance
a
np:Provenance
.
dgn-np:NP50715.RAP4cQVdpRxmdV8Gcv6AU5xpSVkNPgLN2LmzeeMoTQlBQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP50715.RAP4cQVdpRxmdV8Gcv6AU5xpSVkNPgLN2LmzeeMoTQlBQ130_assertion
{
miriam-gene:7039
a
ncit:C16612
.
lld:C0000768
a
ncit:C7057
.
dgn-gda:DGN64c8b0000b79e8e405ec143aaa21a0f8
sio:SIO_000628
miriam-gene:7039
,
lld:C0000768
;
a
sio:SIO_001122
.
}
dgn-np:NP50715.RAP4cQVdpRxmdV8Gcv6AU5xpSVkNPgLN2LmzeeMoTQlBQ130_provenance
{
dgn-np:NP50715.RAP4cQVdpRxmdV8Gcv6AU5xpSVkNPgLN2LmzeeMoTQlBQ130_assertion
dcterms:description
"[While there was a modest increase in the less common C2 allele at the TaqI site in the transforming growth factor alpha (TGF alpha) locus among cleft palate only infants compared with the birth defect controls, the association appeared to reflect an underlying interaction between maternal smoking and infant genotype.]. 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:7702037
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP50715.RAP4cQVdpRxmdV8Gcv6AU5xpSVkNPgLN2LmzeeMoTQlBQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:23+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" .
}