Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP434978.RAgpCKTQmeQT716klQeGO_lFFUtF08HRARFpgdDZr_UGw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP434978.RAgpCKTQmeQT716klQeGO_lFFUtF08HRARFpgdDZr_UGw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP434978.RAgpCKTQmeQT716klQeGO_lFFUtF08HRARFpgdDZr_UGw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP434978.RAgpCKTQmeQT716klQeGO_lFFUtF08HRARFpgdDZr_UGw130_provenance.
- NP434978.RAgpCKTQmeQT716klQeGO_lFFUtF08HRARFpgdDZr_UGw130_assertion description "[Based on the literature and this study we suggest as diagnostic criteria for OFD VI: MTS and one or more of the following: 1) tongue hamartoma(s) and/or additional frenula and/or upper lip notch; 2) mesoaxial polydactyly of one or more hands or feet; 3) hypothalamic hamartoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP434978.RAgpCKTQmeQT716klQeGO_lFFUtF08HRARFpgdDZr_UGw130_provenance.
- NP434978.RAgpCKTQmeQT716klQeGO_lFFUtF08HRARFpgdDZr_UGw130_assertion evidence source_evidence_literature NP434978.RAgpCKTQmeQT716klQeGO_lFFUtF08HRARFpgdDZr_UGw130_provenance.
- NP434978.RAgpCKTQmeQT716klQeGO_lFFUtF08HRARFpgdDZr_UGw130_assertion SIO_000772 22236771 NP434978.RAgpCKTQmeQT716klQeGO_lFFUtF08HRARFpgdDZr_UGw130_provenance.
- NP434978.RAgpCKTQmeQT716klQeGO_lFFUtF08HRARFpgdDZr_UGw130_assertion wasDerivedFrom befree-20140225 NP434978.RAgpCKTQmeQT716klQeGO_lFFUtF08HRARFpgdDZr_UGw130_provenance.
- NP434978.RAgpCKTQmeQT716klQeGO_lFFUtF08HRARFpgdDZr_UGw130_assertion wasGeneratedBy ECO_0000203 NP434978.RAgpCKTQmeQT716klQeGO_lFFUtF08HRARFpgdDZr_UGw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP434978.RAgpCKTQmeQT716klQeGO_lFFUtF08HRARFpgdDZr_UGw130_provenance.