Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP406879.RAyyBrBKOrJFLf3Tf-QaLUPYJ1CNrmgmDZ_6mYWauxbTs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP406879.RAyyBrBKOrJFLf3Tf-QaLUPYJ1CNrmgmDZ_6mYWauxbTs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP406879.RAyyBrBKOrJFLf3Tf-QaLUPYJ1CNrmgmDZ_6mYWauxbTs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP406879.RAyyBrBKOrJFLf3Tf-QaLUPYJ1CNrmgmDZ_6mYWauxbTs130_provenance.
- NP406879.RAyyBrBKOrJFLf3Tf-QaLUPYJ1CNrmgmDZ_6mYWauxbTs130_assertion description "[The nature of the mutation has been considered the major determinant of the phenotype within this group that comprises the otopalatodigital syndromes (OPD1, OPD2) and Melnick-Needles syndrome besides FMD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP406879.RAyyBrBKOrJFLf3Tf-QaLUPYJ1CNrmgmDZ_6mYWauxbTs130_provenance.
- NP406879.RAyyBrBKOrJFLf3Tf-QaLUPYJ1CNrmgmDZ_6mYWauxbTs130_assertion evidence source_evidence_literature NP406879.RAyyBrBKOrJFLf3Tf-QaLUPYJ1CNrmgmDZ_6mYWauxbTs130_provenance.
- NP406879.RAyyBrBKOrJFLf3Tf-QaLUPYJ1CNrmgmDZ_6mYWauxbTs130_assertion SIO_000772 16596676 NP406879.RAyyBrBKOrJFLf3Tf-QaLUPYJ1CNrmgmDZ_6mYWauxbTs130_provenance.
- NP406879.RAyyBrBKOrJFLf3Tf-QaLUPYJ1CNrmgmDZ_6mYWauxbTs130_assertion wasDerivedFrom befree-20150227 NP406879.RAyyBrBKOrJFLf3Tf-QaLUPYJ1CNrmgmDZ_6mYWauxbTs130_provenance.
- NP406879.RAyyBrBKOrJFLf3Tf-QaLUPYJ1CNrmgmDZ_6mYWauxbTs130_assertion wasGeneratedBy ECO_0000203 NP406879.RAyyBrBKOrJFLf3Tf-QaLUPYJ1CNrmgmDZ_6mYWauxbTs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP406879.RAyyBrBKOrJFLf3Tf-QaLUPYJ1CNrmgmDZ_6mYWauxbTs130_provenance.