Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP766616.RA-chAPRNzdbggqaoSyMsHlb1iZ9--LyNHENE__Zo8OF4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP766616.RA-chAPRNzdbggqaoSyMsHlb1iZ9--LyNHENE__Zo8OF4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP766616.RA-chAPRNzdbggqaoSyMsHlb1iZ9--LyNHENE__Zo8OF4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP766616.RA-chAPRNzdbggqaoSyMsHlb1iZ9--LyNHENE__Zo8OF4130_provenance.
- NP766616.RA-chAPRNzdbggqaoSyMsHlb1iZ9--LyNHENE__Zo8OF4130_assertion description "[Two hereditary human leukemia syndromes are severe congenital neutropenia (SCN), caused by mutations in the gene ELA2, encoding the protease neutrophil elastase, and familial platelet disorder with acute myelogenous leukemia (AML), caused by mutations in the gene AML1, encoding the transcription factor core-binding factor alpha (CBFalpha).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP766616.RA-chAPRNzdbggqaoSyMsHlb1iZ9--LyNHENE__Zo8OF4130_provenance.
- NP766616.RA-chAPRNzdbggqaoSyMsHlb1iZ9--LyNHENE__Zo8OF4130_assertion evidence source_evidence_literature NP766616.RA-chAPRNzdbggqaoSyMsHlb1iZ9--LyNHENE__Zo8OF4130_provenance.
- NP766616.RA-chAPRNzdbggqaoSyMsHlb1iZ9--LyNHENE__Zo8OF4130_assertion SIO_000772 14594802 NP766616.RA-chAPRNzdbggqaoSyMsHlb1iZ9--LyNHENE__Zo8OF4130_provenance.
- NP766616.RA-chAPRNzdbggqaoSyMsHlb1iZ9--LyNHENE__Zo8OF4130_assertion wasDerivedFrom befree-20140225 NP766616.RA-chAPRNzdbggqaoSyMsHlb1iZ9--LyNHENE__Zo8OF4130_provenance.
- NP766616.RA-chAPRNzdbggqaoSyMsHlb1iZ9--LyNHENE__Zo8OF4130_assertion wasGeneratedBy ECO_0000203 NP766616.RA-chAPRNzdbggqaoSyMsHlb1iZ9--LyNHENE__Zo8OF4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP766616.RA-chAPRNzdbggqaoSyMsHlb1iZ9--LyNHENE__Zo8OF4130_provenance.