Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP408688.RAK60wqbLfAhBFFNXxLtYllVoUkTZvNd4PuSBWy-xscE8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP408688.RAK60wqbLfAhBFFNXxLtYllVoUkTZvNd4PuSBWy-xscE8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP408688.RAK60wqbLfAhBFFNXxLtYllVoUkTZvNd4PuSBWy-xscE8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP408688.RAK60wqbLfAhBFFNXxLtYllVoUkTZvNd4PuSBWy-xscE8130_provenance.
- NP408688.RAK60wqbLfAhBFFNXxLtYllVoUkTZvNd4PuSBWy-xscE8130_assertion description "[These data indicate that a lack of FMRP leads to cerebellar deficits at both the cellular and behavioral levels and raise the possibility that cerebellar dysfunctions can contribute to motor learning deficits in Fragile X patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP408688.RAK60wqbLfAhBFFNXxLtYllVoUkTZvNd4PuSBWy-xscE8130_provenance.
- NP408688.RAK60wqbLfAhBFFNXxLtYllVoUkTZvNd4PuSBWy-xscE8130_assertion evidence source_evidence_literature NP408688.RAK60wqbLfAhBFFNXxLtYllVoUkTZvNd4PuSBWy-xscE8130_provenance.
- NP408688.RAK60wqbLfAhBFFNXxLtYllVoUkTZvNd4PuSBWy-xscE8130_assertion SIO_000772 16055059 NP408688.RAK60wqbLfAhBFFNXxLtYllVoUkTZvNd4PuSBWy-xscE8130_provenance.
- NP408688.RAK60wqbLfAhBFFNXxLtYllVoUkTZvNd4PuSBWy-xscE8130_assertion wasDerivedFrom befree-20150227 NP408688.RAK60wqbLfAhBFFNXxLtYllVoUkTZvNd4PuSBWy-xscE8130_provenance.
- NP408688.RAK60wqbLfAhBFFNXxLtYllVoUkTZvNd4PuSBWy-xscE8130_assertion wasGeneratedBy ECO_0000203 NP408688.RAK60wqbLfAhBFFNXxLtYllVoUkTZvNd4PuSBWy-xscE8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP408688.RAK60wqbLfAhBFFNXxLtYllVoUkTZvNd4PuSBWy-xscE8130_provenance.