@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP725119.RA3gPP89mqesUPfFtcCqMOMoSez7gYnJAlRwMBL8sV3SY> .
@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:NP725119.RA3gPP89mqesUPfFtcCqMOMoSez7gYnJAlRwMBL8sV3SY130_head {
  this: np:hasAssertion dgn-np:NP725119.RA3gPP89mqesUPfFtcCqMOMoSez7gYnJAlRwMBL8sV3SY130_assertion;
    np:hasProvenance dgn-np:NP725119.RA3gPP89mqesUPfFtcCqMOMoSez7gYnJAlRwMBL8sV3SY130_provenance;
    np:hasPublicationInfo dgn-np:NP725119.RA3gPP89mqesUPfFtcCqMOMoSez7gYnJAlRwMBL8sV3SY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP725119.RA3gPP89mqesUPfFtcCqMOMoSez7gYnJAlRwMBL8sV3SY130_assertion a np:Assertion .
  
  dgn-np:NP725119.RA3gPP89mqesUPfFtcCqMOMoSez7gYnJAlRwMBL8sV3SY130_provenance a np:Provenance .
  
  dgn-np:NP725119.RA3gPP89mqesUPfFtcCqMOMoSez7gYnJAlRwMBL8sV3SY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP725119.RA3gPP89mqesUPfFtcCqMOMoSez7gYnJAlRwMBL8sV3SY130_assertion {
  miriam-gene:657 a ncit:C16612 .
  
  lld:C0039075 a ncit:C7057 .
  
  dgn-gda:DGN7eeae492b805228d3f0021b35e4093f6 sio:SIO_000628 miriam-gene:657, lld:C0039075;
    a sio:SIO_001121 .
}

dgn-np:NP725119.RA3gPP89mqesUPfFtcCqMOMoSez7gYnJAlRwMBL8sV3SY130_provenance {
  dgn-np:NP725119.RA3gPP89mqesUPfFtcCqMOMoSez7gYnJAlRwMBL8sV3SY130_assertion dcterms:description
      "[Biosensor interaction analyses revealed loss of binding to BMPR1A and BMPR1B ectodomains for the L441P mutant, whereas the R438L mutant showed normal binding to BMPR1B but increased binding to BMPR1A, the receptor normally activated by BMP2.]. 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:16127465;
    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:NP725119.RA3gPP89mqesUPfFtcCqMOMoSez7gYnJAlRwMBL8sV3SY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:20+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" .
}