Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP291011.RA25qt16zgqQbFp4NCKBF-5lfE-xct5fkaIW-d2mxDWTI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP291011.RA25qt16zgqQbFp4NCKBF-5lfE-xct5fkaIW-d2mxDWTI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP291011.RA25qt16zgqQbFp4NCKBF-5lfE-xct5fkaIW-d2mxDWTI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP291011.RA25qt16zgqQbFp4NCKBF-5lfE-xct5fkaIW-d2mxDWTI130_provenance.
- NP291011.RA25qt16zgqQbFp4NCKBF-5lfE-xct5fkaIW-d2mxDWTI130_assertion description "[In conclusion, a novel DAX-1 mutation was detected in two family members with different phenotype: one live infant with adrenal hypoplasia, his mother, and probably his dead brother.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP291011.RA25qt16zgqQbFp4NCKBF-5lfE-xct5fkaIW-d2mxDWTI130_provenance.
- NP291011.RA25qt16zgqQbFp4NCKBF-5lfE-xct5fkaIW-d2mxDWTI130_assertion evidence source_evidence_literature NP291011.RA25qt16zgqQbFp4NCKBF-5lfE-xct5fkaIW-d2mxDWTI130_provenance.
- NP291011.RA25qt16zgqQbFp4NCKBF-5lfE-xct5fkaIW-d2mxDWTI130_assertion SIO_000772 18038713 NP291011.RA25qt16zgqQbFp4NCKBF-5lfE-xct5fkaIW-d2mxDWTI130_provenance.
- NP291011.RA25qt16zgqQbFp4NCKBF-5lfE-xct5fkaIW-d2mxDWTI130_assertion wasDerivedFrom befree-20140225 NP291011.RA25qt16zgqQbFp4NCKBF-5lfE-xct5fkaIW-d2mxDWTI130_provenance.
- NP291011.RA25qt16zgqQbFp4NCKBF-5lfE-xct5fkaIW-d2mxDWTI130_assertion wasGeneratedBy ECO_0000203 NP291011.RA25qt16zgqQbFp4NCKBF-5lfE-xct5fkaIW-d2mxDWTI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP291011.RA25qt16zgqQbFp4NCKBF-5lfE-xct5fkaIW-d2mxDWTI130_provenance.