Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1119691.RA_22fTK4inLOZGZnEB75gIHN3ditTN1X91w4d2SfDcOQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1119691.RA_22fTK4inLOZGZnEB75gIHN3ditTN1X91w4d2SfDcOQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1119691.RA_22fTK4inLOZGZnEB75gIHN3ditTN1X91w4d2SfDcOQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1119691.RA_22fTK4inLOZGZnEB75gIHN3ditTN1X91w4d2SfDcOQ130_provenance.
- NP1119691.RA_22fTK4inLOZGZnEB75gIHN3ditTN1X91w4d2SfDcOQ130_assertion description "[This study aims to identify signatures of miR associated with hereditary, BRCA1 or BRCA2 mutation positive breast cancer (BC), and non-hereditary BC, either sporadic (SBC) or non-informative (BRCAX).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1119691.RA_22fTK4inLOZGZnEB75gIHN3ditTN1X91w4d2SfDcOQ130_provenance.
- NP1119691.RA_22fTK4inLOZGZnEB75gIHN3ditTN1X91w4d2SfDcOQ130_assertion evidence source_evidence_literature NP1119691.RA_22fTK4inLOZGZnEB75gIHN3ditTN1X91w4d2SfDcOQ130_provenance.
- NP1119691.RA_22fTK4inLOZGZnEB75gIHN3ditTN1X91w4d2SfDcOQ130_assertion SIO_000772 24129975 NP1119691.RA_22fTK4inLOZGZnEB75gIHN3ditTN1X91w4d2SfDcOQ130_provenance.
- NP1119691.RA_22fTK4inLOZGZnEB75gIHN3ditTN1X91w4d2SfDcOQ130_assertion wasDerivedFrom befree-2016 NP1119691.RA_22fTK4inLOZGZnEB75gIHN3ditTN1X91w4d2SfDcOQ130_provenance.
- NP1119691.RA_22fTK4inLOZGZnEB75gIHN3ditTN1X91w4d2SfDcOQ130_assertion wasGeneratedBy ECO_0000203 NP1119691.RA_22fTK4inLOZGZnEB75gIHN3ditTN1X91w4d2SfDcOQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1119691.RA_22fTK4inLOZGZnEB75gIHN3ditTN1X91w4d2SfDcOQ130_provenance.