@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP514318.RAPcrqbwYnj0X6saE9w1iz8a8Dm0aN3aqAUIPuCgcTDBU
> .
@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:NP514318.RAPcrqbwYnj0X6saE9w1iz8a8Dm0aN3aqAUIPuCgcTDBU130_head
{
this:
np:hasAssertion
dgn-np:NP514318.RAPcrqbwYnj0X6saE9w1iz8a8Dm0aN3aqAUIPuCgcTDBU130_assertion
;
np:hasProvenance
dgn-np:NP514318.RAPcrqbwYnj0X6saE9w1iz8a8Dm0aN3aqAUIPuCgcTDBU130_provenance
;
np:hasPublicationInfo
dgn-np:NP514318.RAPcrqbwYnj0X6saE9w1iz8a8Dm0aN3aqAUIPuCgcTDBU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP514318.RAPcrqbwYnj0X6saE9w1iz8a8Dm0aN3aqAUIPuCgcTDBU130_assertion
a
np:Assertion
.
dgn-np:NP514318.RAPcrqbwYnj0X6saE9w1iz8a8Dm0aN3aqAUIPuCgcTDBU130_provenance
a
np:Provenance
.
dgn-np:NP514318.RAPcrqbwYnj0X6saE9w1iz8a8Dm0aN3aqAUIPuCgcTDBU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP514318.RAPcrqbwYnj0X6saE9w1iz8a8Dm0aN3aqAUIPuCgcTDBU130_assertion
{
miriam-gene:6927
a
ncit:C16612
.
lld:C0496870
a
ncit:C7057
.
dgn-gda:DGN3c03c63f3f50355aeb4412881da9fbb3
sio:SIO_000628
miriam-gene:6927
,
lld:C0496870
;
a
sio:SIO_001121
.
}
dgn-np:NP514318.RAPcrqbwYnj0X6saE9w1iz8a8Dm0aN3aqAUIPuCgcTDBU130_provenance
{
dgn-np:NP514318.RAPcrqbwYnj0X6saE9w1iz8a8Dm0aN3aqAUIPuCgcTDBU130_assertion
dcterms:description
"[Biallelic inactivating mutations of HNF1A have been frequently identified in hepatocellular adenomas (HCA), rare benign liver tumors usually developed in women under oral contraceptives, and in rare cases of hepatocellular carcinomas developed in non-cirrhotic liver.]. 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:21975049
;
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:NP514318.RAPcrqbwYnj0X6saE9w1iz8a8Dm0aN3aqAUIPuCgcTDBU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:06+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" .
}