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- NP318937.RAD6D3yALifQLDRiVn0mn__oa7NULO1YTXASXpvGu7q14130_assertion type Assertion NP318937.RAD6D3yALifQLDRiVn0mn__oa7NULO1YTXASXpvGu7q14130_head.
- NP318937.RAD6D3yALifQLDRiVn0mn__oa7NULO1YTXASXpvGu7q14130_assertion wasGeneratedBy ECO_0000203 NP318937.RAD6D3yALifQLDRiVn0mn__oa7NULO1YTXASXpvGu7q14130_provenance.
- NP318937.RAD6D3yALifQLDRiVn0mn__oa7NULO1YTXASXpvGu7q14130_assertion wasDerivedFrom befree-20150227 NP318937.RAD6D3yALifQLDRiVn0mn__oa7NULO1YTXASXpvGu7q14130_provenance.
- NP318937.RAD6D3yALifQLDRiVn0mn__oa7NULO1YTXASXpvGu7q14130_assertion SIO_000772 11951178 NP318937.RAD6D3yALifQLDRiVn0mn__oa7NULO1YTXASXpvGu7q14130_provenance.
- NP318937.RAD6D3yALifQLDRiVn0mn__oa7NULO1YTXASXpvGu7q14130_assertion evidence source_evidence_literature NP318937.RAD6D3yALifQLDRiVn0mn__oa7NULO1YTXASXpvGu7q14130_provenance.
- NP318937.RAD6D3yALifQLDRiVn0mn__oa7NULO1YTXASXpvGu7q14130_assertion description "[In addition, patients with sporadic amyotrophic lateral sclerosis who had a homozygous CNTF gene defect showed significantly earlier disease onset but did not show a significant difference in disease duration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP318937.RAD6D3yALifQLDRiVn0mn__oa7NULO1YTXASXpvGu7q14130_provenance.