Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP926777.RA_DTFzW56EMkwZJjigHomyqV3mvGUJ-cIvDR-CexvFm4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP926777.RA_DTFzW56EMkwZJjigHomyqV3mvGUJ-cIvDR-CexvFm4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP926777.RA_DTFzW56EMkwZJjigHomyqV3mvGUJ-cIvDR-CexvFm4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP926777.RA_DTFzW56EMkwZJjigHomyqV3mvGUJ-cIvDR-CexvFm4130_provenance.
- NP926777.RA_DTFzW56EMkwZJjigHomyqV3mvGUJ-cIvDR-CexvFm4130_assertion description "[The heterozygous germline mutation of runt-related protein 2 (RUNX2) causes cleidocranial dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP926777.RA_DTFzW56EMkwZJjigHomyqV3mvGUJ-cIvDR-CexvFm4130_provenance.
- NP926777.RA_DTFzW56EMkwZJjigHomyqV3mvGUJ-cIvDR-CexvFm4130_assertion evidence source_evidence_literature NP926777.RA_DTFzW56EMkwZJjigHomyqV3mvGUJ-cIvDR-CexvFm4130_provenance.
- NP926777.RA_DTFzW56EMkwZJjigHomyqV3mvGUJ-cIvDR-CexvFm4130_assertion SIO_000772 21951664 NP926777.RA_DTFzW56EMkwZJjigHomyqV3mvGUJ-cIvDR-CexvFm4130_provenance.
- NP926777.RA_DTFzW56EMkwZJjigHomyqV3mvGUJ-cIvDR-CexvFm4130_assertion wasDerivedFrom befree-2016 NP926777.RA_DTFzW56EMkwZJjigHomyqV3mvGUJ-cIvDR-CexvFm4130_provenance.
- NP926777.RA_DTFzW56EMkwZJjigHomyqV3mvGUJ-cIvDR-CexvFm4130_assertion wasGeneratedBy ECO_0000203 NP926777.RA_DTFzW56EMkwZJjigHomyqV3mvGUJ-cIvDR-CexvFm4130_provenance.
- befree-2016 importedOn "2016-02-19" NP926777.RA_DTFzW56EMkwZJjigHomyqV3mvGUJ-cIvDR-CexvFm4130_provenance.