Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP191987.RA_ehf5pPyc8BU6DcJkDk4GhDCUgHysqnCwhfIL2_MSUQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP191987.RA_ehf5pPyc8BU6DcJkDk4GhDCUgHysqnCwhfIL2_MSUQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP191987.RA_ehf5pPyc8BU6DcJkDk4GhDCUgHysqnCwhfIL2_MSUQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP191987.RA_ehf5pPyc8BU6DcJkDk4GhDCUgHysqnCwhfIL2_MSUQ130_provenance.
- NP191987.RA_ehf5pPyc8BU6DcJkDk4GhDCUgHysqnCwhfIL2_MSUQ130_assertion description "[Left-right axis malformations associated with mutations in ACVR2B, the gene for human activin receptor type IIB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP191987.RA_ehf5pPyc8BU6DcJkDk4GhDCUgHysqnCwhfIL2_MSUQ130_provenance.
- NP191987.RA_ehf5pPyc8BU6DcJkDk4GhDCUgHysqnCwhfIL2_MSUQ130_assertion evidence source_evidence_literature NP191987.RA_ehf5pPyc8BU6DcJkDk4GhDCUgHysqnCwhfIL2_MSUQ130_provenance.
- NP191987.RA_ehf5pPyc8BU6DcJkDk4GhDCUgHysqnCwhfIL2_MSUQ130_assertion SIO_000772 9916847 NP191987.RA_ehf5pPyc8BU6DcJkDk4GhDCUgHysqnCwhfIL2_MSUQ130_provenance.
- NP191987.RA_ehf5pPyc8BU6DcJkDk4GhDCUgHysqnCwhfIL2_MSUQ130_assertion wasDerivedFrom gad-20150221 NP191987.RA_ehf5pPyc8BU6DcJkDk4GhDCUgHysqnCwhfIL2_MSUQ130_provenance.
- NP191987.RA_ehf5pPyc8BU6DcJkDk4GhDCUgHysqnCwhfIL2_MSUQ130_assertion wasGeneratedBy ECO_0000203 NP191987.RA_ehf5pPyc8BU6DcJkDk4GhDCUgHysqnCwhfIL2_MSUQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP191987.RA_ehf5pPyc8BU6DcJkDk4GhDCUgHysqnCwhfIL2_MSUQ130_provenance.