Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP341778.RA08ib4LtBvpMBbBdjw68zpvHqmKVVmjlAEhRD_OatSMk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP341778.RA08ib4LtBvpMBbBdjw68zpvHqmKVVmjlAEhRD_OatSMk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP341778.RA08ib4LtBvpMBbBdjw68zpvHqmKVVmjlAEhRD_OatSMk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP341778.RA08ib4LtBvpMBbBdjw68zpvHqmKVVmjlAEhRD_OatSMk130_provenance.
- NP341778.RA08ib4LtBvpMBbBdjw68zpvHqmKVVmjlAEhRD_OatSMk130_assertion description "[Fanconi anemia (FA) is an autosomal recessive chromosomal instability disorder caused by mutations in one of seven known genes (FANCA,C,D2,E,F,G and BRCA2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP341778.RA08ib4LtBvpMBbBdjw68zpvHqmKVVmjlAEhRD_OatSMk130_provenance.
- NP341778.RA08ib4LtBvpMBbBdjw68zpvHqmKVVmjlAEhRD_OatSMk130_assertion evidence source_evidence_literature NP341778.RA08ib4LtBvpMBbBdjw68zpvHqmKVVmjlAEhRD_OatSMk130_provenance.
- NP341778.RA08ib4LtBvpMBbBdjw68zpvHqmKVVmjlAEhRD_OatSMk130_assertion SIO_000772 14749703 NP341778.RA08ib4LtBvpMBbBdjw68zpvHqmKVVmjlAEhRD_OatSMk130_provenance.
- NP341778.RA08ib4LtBvpMBbBdjw68zpvHqmKVVmjlAEhRD_OatSMk130_assertion wasDerivedFrom befree-20140225 NP341778.RA08ib4LtBvpMBbBdjw68zpvHqmKVVmjlAEhRD_OatSMk130_provenance.
- NP341778.RA08ib4LtBvpMBbBdjw68zpvHqmKVVmjlAEhRD_OatSMk130_assertion wasGeneratedBy ECO_0000203 NP341778.RA08ib4LtBvpMBbBdjw68zpvHqmKVVmjlAEhRD_OatSMk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP341778.RA08ib4LtBvpMBbBdjw68zpvHqmKVVmjlAEhRD_OatSMk130_provenance.