Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP168783.RASuo2cUNad9C94uhSDGbdSwV00r3WD6T8gZ_zpJAngvI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP168783.RASuo2cUNad9C94uhSDGbdSwV00r3WD6T8gZ_zpJAngvI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP168783.RASuo2cUNad9C94uhSDGbdSwV00r3WD6T8gZ_zpJAngvI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP168783.RASuo2cUNad9C94uhSDGbdSwV00r3WD6T8gZ_zpJAngvI130_provenance.
- NP168783.RASuo2cUNad9C94uhSDGbdSwV00r3WD6T8gZ_zpJAngvI130_assertion description "[Myotonic dystrophy type 2 (DM2) is caused by CCTG-repeat expansions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP168783.RASuo2cUNad9C94uhSDGbdSwV00r3WD6T8gZ_zpJAngvI130_provenance.
- NP168783.RASuo2cUNad9C94uhSDGbdSwV00r3WD6T8gZ_zpJAngvI130_assertion evidence source_evidence_literature NP168783.RASuo2cUNad9C94uhSDGbdSwV00r3WD6T8gZ_zpJAngvI130_provenance.
- NP168783.RASuo2cUNad9C94uhSDGbdSwV00r3WD6T8gZ_zpJAngvI130_assertion SIO_000772 23097607 NP168783.RASuo2cUNad9C94uhSDGbdSwV00r3WD6T8gZ_zpJAngvI130_provenance.
- NP168783.RASuo2cUNad9C94uhSDGbdSwV00r3WD6T8gZ_zpJAngvI130_assertion wasDerivedFrom befree-20140225 NP168783.RASuo2cUNad9C94uhSDGbdSwV00r3WD6T8gZ_zpJAngvI130_provenance.
- NP168783.RASuo2cUNad9C94uhSDGbdSwV00r3WD6T8gZ_zpJAngvI130_assertion wasGeneratedBy ECO_0000203 NP168783.RASuo2cUNad9C94uhSDGbdSwV00r3WD6T8gZ_zpJAngvI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP168783.RASuo2cUNad9C94uhSDGbdSwV00r3WD6T8gZ_zpJAngvI130_provenance.