Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP122956.RAEJYYtRmD_gYlldJUFt7Q2Z86nXrC4bRH72nNbIs4-Eg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP122956.RAEJYYtRmD_gYlldJUFt7Q2Z86nXrC4bRH72nNbIs4-Eg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP122956.RAEJYYtRmD_gYlldJUFt7Q2Z86nXrC4bRH72nNbIs4-Eg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP122956.RAEJYYtRmD_gYlldJUFt7Q2Z86nXrC4bRH72nNbIs4-Eg130_provenance.
- NP122956.RAEJYYtRmD_gYlldJUFt7Q2Z86nXrC4bRH72nNbIs4-Eg130_assertion description "[a heterozygous factor V Leiden mutation was found in nine patients (17.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP122956.RAEJYYtRmD_gYlldJUFt7Q2Z86nXrC4bRH72nNbIs4-Eg130_provenance.
- NP122956.RAEJYYtRmD_gYlldJUFt7Q2Z86nXrC4bRH72nNbIs4-Eg130_assertion evidence source_evidence_literature NP122956.RAEJYYtRmD_gYlldJUFt7Q2Z86nXrC4bRH72nNbIs4-Eg130_provenance.
- NP122956.RAEJYYtRmD_gYlldJUFt7Q2Z86nXrC4bRH72nNbIs4-Eg130_assertion SIO_000772 18469551 NP122956.RAEJYYtRmD_gYlldJUFt7Q2Z86nXrC4bRH72nNbIs4-Eg130_provenance.
- NP122956.RAEJYYtRmD_gYlldJUFt7Q2Z86nXrC4bRH72nNbIs4-Eg130_assertion wasDerivedFrom gad-20150221 NP122956.RAEJYYtRmD_gYlldJUFt7Q2Z86nXrC4bRH72nNbIs4-Eg130_provenance.
- NP122956.RAEJYYtRmD_gYlldJUFt7Q2Z86nXrC4bRH72nNbIs4-Eg130_assertion wasGeneratedBy ECO_0000203 NP122956.RAEJYYtRmD_gYlldJUFt7Q2Z86nXrC4bRH72nNbIs4-Eg130_provenance.
- gad-20150221 importedOn "2015-02-21" NP122956.RAEJYYtRmD_gYlldJUFt7Q2Z86nXrC4bRH72nNbIs4-Eg130_provenance.