Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP865298.RAD9ruAtZX8K-R6CCFxMbqLWMSADYtQ3dOXRwLRHPi1H8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP865298.RAD9ruAtZX8K-R6CCFxMbqLWMSADYtQ3dOXRwLRHPi1H8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP865298.RAD9ruAtZX8K-R6CCFxMbqLWMSADYtQ3dOXRwLRHPi1H8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP865298.RAD9ruAtZX8K-R6CCFxMbqLWMSADYtQ3dOXRwLRHPi1H8130_provenance.
- befree-2016 importedOn "2016-02-19" NP865298.RAD9ruAtZX8K-R6CCFxMbqLWMSADYtQ3dOXRwLRHPi1H8130_provenance.
- NP865298.RAD9ruAtZX8K-R6CCFxMbqLWMSADYtQ3dOXRwLRHPi1H8130_assertion wasGeneratedBy ECO_0000203 NP865298.RAD9ruAtZX8K-R6CCFxMbqLWMSADYtQ3dOXRwLRHPi1H8130_provenance.
- NP865298.RAD9ruAtZX8K-R6CCFxMbqLWMSADYtQ3dOXRwLRHPi1H8130_assertion wasDerivedFrom befree-2016 NP865298.RAD9ruAtZX8K-R6CCFxMbqLWMSADYtQ3dOXRwLRHPi1H8130_provenance.
- NP865298.RAD9ruAtZX8K-R6CCFxMbqLWMSADYtQ3dOXRwLRHPi1H8130_assertion SIO_000772 21233719 NP865298.RAD9ruAtZX8K-R6CCFxMbqLWMSADYtQ3dOXRwLRHPi1H8130_provenance.
- NP865298.RAD9ruAtZX8K-R6CCFxMbqLWMSADYtQ3dOXRwLRHPi1H8130_assertion evidence source_evidence_literature NP865298.RAD9ruAtZX8K-R6CCFxMbqLWMSADYtQ3dOXRwLRHPi1H8130_provenance.
- NP865298.RAD9ruAtZX8K-R6CCFxMbqLWMSADYtQ3dOXRwLRHPi1H8130_assertion description "[Currently used molecular techniques cannot detect about 5% of spinal muscular atrophy carriers with a cis configuration or individuals with SMN1 sequence mutations and de novo deletions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP865298.RAD9ruAtZX8K-R6CCFxMbqLWMSADYtQ3dOXRwLRHPi1H8130_provenance.