Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP886530.RAYl-FpFct976vt9lYXnmIhHp87DSGS9C5b-KzSFBl7dk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP886530.RAYl-FpFct976vt9lYXnmIhHp87DSGS9C5b-KzSFBl7dk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP886530.RAYl-FpFct976vt9lYXnmIhHp87DSGS9C5b-KzSFBl7dk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP886530.RAYl-FpFct976vt9lYXnmIhHp87DSGS9C5b-KzSFBl7dk130_provenance.
- befree-2016 importedOn "2016-02-19" NP886530.RAYl-FpFct976vt9lYXnmIhHp87DSGS9C5b-KzSFBl7dk130_provenance.
- NP886530.RAYl-FpFct976vt9lYXnmIhHp87DSGS9C5b-KzSFBl7dk130_assertion wasGeneratedBy ECO_0000203 NP886530.RAYl-FpFct976vt9lYXnmIhHp87DSGS9C5b-KzSFBl7dk130_provenance.
- NP886530.RAYl-FpFct976vt9lYXnmIhHp87DSGS9C5b-KzSFBl7dk130_assertion wasDerivedFrom befree-2016 NP886530.RAYl-FpFct976vt9lYXnmIhHp87DSGS9C5b-KzSFBl7dk130_provenance.
- NP886530.RAYl-FpFct976vt9lYXnmIhHp87DSGS9C5b-KzSFBl7dk130_assertion SIO_000772 2148653 NP886530.RAYl-FpFct976vt9lYXnmIhHp87DSGS9C5b-KzSFBl7dk130_provenance.
- NP886530.RAYl-FpFct976vt9lYXnmIhHp87DSGS9C5b-KzSFBl7dk130_assertion evidence source_evidence_literature NP886530.RAYl-FpFct976vt9lYXnmIhHp87DSGS9C5b-KzSFBl7dk130_provenance.
- NP886530.RAYl-FpFct976vt9lYXnmIhHp87DSGS9C5b-KzSFBl7dk130_assertion description "[In a group of 37 consecutive patients with arterial occlusive disease presenting before the age of 45, three patients were found heterozygous for hereditary protein S deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP886530.RAYl-FpFct976vt9lYXnmIhHp87DSGS9C5b-KzSFBl7dk130_provenance.