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- source_evidence_literature type ECO_0000212 NP710196.RAVjXwZ1Ouc3b1YJdRwfUrj6fXwjFgwFS_lfSFFZ4NB0c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP710196.RAVjXwZ1Ouc3b1YJdRwfUrj6fXwjFgwFS_lfSFFZ4NB0c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP710196.RAVjXwZ1Ouc3b1YJdRwfUrj6fXwjFgwFS_lfSFFZ4NB0c130_provenance.
- NP710196.RAVjXwZ1Ouc3b1YJdRwfUrj6fXwjFgwFS_lfSFFZ4NB0c130_assertion description "[The provided genomic structure of SPG7 should facilitate the screening for mutations in this gene in patients with HSP and other related mitochondrial disease syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710196.RAVjXwZ1Ouc3b1YJdRwfUrj6fXwjFgwFS_lfSFFZ4NB0c130_provenance.
- NP710196.RAVjXwZ1Ouc3b1YJdRwfUrj6fXwjFgwFS_lfSFFZ4NB0c130_assertion evidence source_evidence_literature NP710196.RAVjXwZ1Ouc3b1YJdRwfUrj6fXwjFgwFS_lfSFFZ4NB0c130_provenance.
- NP710196.RAVjXwZ1Ouc3b1YJdRwfUrj6fXwjFgwFS_lfSFFZ4NB0c130_assertion SIO_000772 10480368 NP710196.RAVjXwZ1Ouc3b1YJdRwfUrj6fXwjFgwFS_lfSFFZ4NB0c130_provenance.
- NP710196.RAVjXwZ1Ouc3b1YJdRwfUrj6fXwjFgwFS_lfSFFZ4NB0c130_assertion wasDerivedFrom befree-20150227 NP710196.RAVjXwZ1Ouc3b1YJdRwfUrj6fXwjFgwFS_lfSFFZ4NB0c130_provenance.
- NP710196.RAVjXwZ1Ouc3b1YJdRwfUrj6fXwjFgwFS_lfSFFZ4NB0c130_assertion wasGeneratedBy ECO_0000203 NP710196.RAVjXwZ1Ouc3b1YJdRwfUrj6fXwjFgwFS_lfSFFZ4NB0c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP710196.RAVjXwZ1Ouc3b1YJdRwfUrj6fXwjFgwFS_lfSFFZ4NB0c130_provenance.