Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP395907.RAxzXs3mpq7g7KN4_XhFm-LB7RR0lwDl08cia1JzRnoDA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP395907.RAxzXs3mpq7g7KN4_XhFm-LB7RR0lwDl08cia1JzRnoDA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP395907.RAxzXs3mpq7g7KN4_XhFm-LB7RR0lwDl08cia1JzRnoDA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP395907.RAxzXs3mpq7g7KN4_XhFm-LB7RR0lwDl08cia1JzRnoDA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP395907.RAxzXs3mpq7g7KN4_XhFm-LB7RR0lwDl08cia1JzRnoDA130_provenance.
- NP395907.RAxzXs3mpq7g7KN4_XhFm-LB7RR0lwDl08cia1JzRnoDA130_assertion wasGeneratedBy ECO_0000203 NP395907.RAxzXs3mpq7g7KN4_XhFm-LB7RR0lwDl08cia1JzRnoDA130_provenance.
- NP395907.RAxzXs3mpq7g7KN4_XhFm-LB7RR0lwDl08cia1JzRnoDA130_assertion wasDerivedFrom befree-20150227 NP395907.RAxzXs3mpq7g7KN4_XhFm-LB7RR0lwDl08cia1JzRnoDA130_provenance.
- NP395907.RAxzXs3mpq7g7KN4_XhFm-LB7RR0lwDl08cia1JzRnoDA130_assertion SIO_000772 23133647 NP395907.RAxzXs3mpq7g7KN4_XhFm-LB7RR0lwDl08cia1JzRnoDA130_provenance.
- NP395907.RAxzXs3mpq7g7KN4_XhFm-LB7RR0lwDl08cia1JzRnoDA130_assertion evidence source_evidence_literature NP395907.RAxzXs3mpq7g7KN4_XhFm-LB7RR0lwDl08cia1JzRnoDA130_provenance.
- NP395907.RAxzXs3mpq7g7KN4_XhFm-LB7RR0lwDl08cia1JzRnoDA130_assertion description "[WMS is characterized by short limbs, joint stiffness and ocular defects, whilst fibrillin-1 AD and GD have severe short stature, joint defects and thickened skin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP395907.RAxzXs3mpq7g7KN4_XhFm-LB7RR0lwDl08cia1JzRnoDA130_provenance.