Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP625458.RA1uHFv7lFaXy2WUvYhTJlFpp642kEkLv9I0Xs8kyb4KE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP625458.RA1uHFv7lFaXy2WUvYhTJlFpp642kEkLv9I0Xs8kyb4KE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP625458.RA1uHFv7lFaXy2WUvYhTJlFpp642kEkLv9I0Xs8kyb4KE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP625458.RA1uHFv7lFaXy2WUvYhTJlFpp642kEkLv9I0Xs8kyb4KE130_provenance.
- NP625458.RA1uHFv7lFaXy2WUvYhTJlFpp642kEkLv9I0Xs8kyb4KE130_assertion description "[Two patients had paired mutations in the MVK gene (genotypes V377I/V377I and V377I/S135L) and displayed typical features of BD and MKD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP625458.RA1uHFv7lFaXy2WUvYhTJlFpp642kEkLv9I0Xs8kyb4KE130_provenance.
- NP625458.RA1uHFv7lFaXy2WUvYhTJlFpp642kEkLv9I0Xs8kyb4KE130_assertion evidence source_evidence_literature NP625458.RA1uHFv7lFaXy2WUvYhTJlFpp642kEkLv9I0Xs8kyb4KE130_provenance.
- NP625458.RA1uHFv7lFaXy2WUvYhTJlFpp642kEkLv9I0Xs8kyb4KE130_assertion SIO_000772 17213252 NP625458.RA1uHFv7lFaXy2WUvYhTJlFpp642kEkLv9I0Xs8kyb4KE130_provenance.
- NP625458.RA1uHFv7lFaXy2WUvYhTJlFpp642kEkLv9I0Xs8kyb4KE130_assertion wasDerivedFrom befree-20140225 NP625458.RA1uHFv7lFaXy2WUvYhTJlFpp642kEkLv9I0Xs8kyb4KE130_provenance.
- NP625458.RA1uHFv7lFaXy2WUvYhTJlFpp642kEkLv9I0Xs8kyb4KE130_assertion wasGeneratedBy ECO_0000203 NP625458.RA1uHFv7lFaXy2WUvYhTJlFpp642kEkLv9I0Xs8kyb4KE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP625458.RA1uHFv7lFaXy2WUvYhTJlFpp642kEkLv9I0Xs8kyb4KE130_provenance.