Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP604245.RA_MPeFXFjnVoP-9LKMU32MVV-bsvjbsChk3NKGiDjLmw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP604245.RA_MPeFXFjnVoP-9LKMU32MVV-bsvjbsChk3NKGiDjLmw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP604245.RA_MPeFXFjnVoP-9LKMU32MVV-bsvjbsChk3NKGiDjLmw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP604245.RA_MPeFXFjnVoP-9LKMU32MVV-bsvjbsChk3NKGiDjLmw130_provenance.
- NP604245.RA_MPeFXFjnVoP-9LKMU32MVV-bsvjbsChk3NKGiDjLmw130_assertion description "[A novel dominant negative mutation of OTX2 associated with combined pituitary hormone deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP604245.RA_MPeFXFjnVoP-9LKMU32MVV-bsvjbsChk3NKGiDjLmw130_provenance.
- NP604245.RA_MPeFXFjnVoP-9LKMU32MVV-bsvjbsChk3NKGiDjLmw130_assertion evidence source_evidence_literature NP604245.RA_MPeFXFjnVoP-9LKMU32MVV-bsvjbsChk3NKGiDjLmw130_provenance.
- NP604245.RA_MPeFXFjnVoP-9LKMU32MVV-bsvjbsChk3NKGiDjLmw130_assertion SIO_000772 18728160 NP604245.RA_MPeFXFjnVoP-9LKMU32MVV-bsvjbsChk3NKGiDjLmw130_provenance.
- NP604245.RA_MPeFXFjnVoP-9LKMU32MVV-bsvjbsChk3NKGiDjLmw130_assertion wasDerivedFrom befree-20150227 NP604245.RA_MPeFXFjnVoP-9LKMU32MVV-bsvjbsChk3NKGiDjLmw130_provenance.
- NP604245.RA_MPeFXFjnVoP-9LKMU32MVV-bsvjbsChk3NKGiDjLmw130_assertion wasGeneratedBy ECO_0000203 NP604245.RA_MPeFXFjnVoP-9LKMU32MVV-bsvjbsChk3NKGiDjLmw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP604245.RA_MPeFXFjnVoP-9LKMU32MVV-bsvjbsChk3NKGiDjLmw130_provenance.