Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP530260.RA8mUlhRpOTZOXmeUp4pJMmi9BvKGNljFBBIOkI7t6PDI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP530260.RA8mUlhRpOTZOXmeUp4pJMmi9BvKGNljFBBIOkI7t6PDI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP530260.RA8mUlhRpOTZOXmeUp4pJMmi9BvKGNljFBBIOkI7t6PDI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP530260.RA8mUlhRpOTZOXmeUp4pJMmi9BvKGNljFBBIOkI7t6PDI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP530260.RA8mUlhRpOTZOXmeUp4pJMmi9BvKGNljFBBIOkI7t6PDI130_provenance.
- NP530260.RA8mUlhRpOTZOXmeUp4pJMmi9BvKGNljFBBIOkI7t6PDI130_assertion wasGeneratedBy ECO_0000203 NP530260.RA8mUlhRpOTZOXmeUp4pJMmi9BvKGNljFBBIOkI7t6PDI130_provenance.
- NP530260.RA8mUlhRpOTZOXmeUp4pJMmi9BvKGNljFBBIOkI7t6PDI130_assertion wasDerivedFrom befree-20150227 NP530260.RA8mUlhRpOTZOXmeUp4pJMmi9BvKGNljFBBIOkI7t6PDI130_provenance.
- NP530260.RA8mUlhRpOTZOXmeUp4pJMmi9BvKGNljFBBIOkI7t6PDI130_assertion SIO_000772 12467726 NP530260.RA8mUlhRpOTZOXmeUp4pJMmi9BvKGNljFBBIOkI7t6PDI130_provenance.
- NP530260.RA8mUlhRpOTZOXmeUp4pJMmi9BvKGNljFBBIOkI7t6PDI130_assertion evidence source_evidence_literature NP530260.RA8mUlhRpOTZOXmeUp4pJMmi9BvKGNljFBBIOkI7t6PDI130_provenance.
- NP530260.RA8mUlhRpOTZOXmeUp4pJMmi9BvKGNljFBBIOkI7t6PDI130_assertion description "[These patients constituted a particular form of congenital muscular dystrophy with a combination of severe motor delay, mental retardation, partial merosin deficiency and cerebellar cysts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP530260.RA8mUlhRpOTZOXmeUp4pJMmi9BvKGNljFBBIOkI7t6PDI130_provenance.