Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP674706.RAlZ5xFxABtnNhXbOa4RjeXmPGWeiWGnsEq2rNo4NtJzg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP674706.RAlZ5xFxABtnNhXbOa4RjeXmPGWeiWGnsEq2rNo4NtJzg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP674706.RAlZ5xFxABtnNhXbOa4RjeXmPGWeiWGnsEq2rNo4NtJzg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP674706.RAlZ5xFxABtnNhXbOa4RjeXmPGWeiWGnsEq2rNo4NtJzg130_provenance.
- NP674706.RAlZ5xFxABtnNhXbOa4RjeXmPGWeiWGnsEq2rNo4NtJzg130_assertion description "[The three-dimensional solution structure of the p63 sterile alpha-motif (SAM) domain (residues 505-579), a region crucial to explaining the human genetic disease ankyloblepharonectodermal dysplasia-clefting syndrome (AEC), has been determined by nuclear magnetic resonance spectroscopy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674706.RAlZ5xFxABtnNhXbOa4RjeXmPGWeiWGnsEq2rNo4NtJzg130_provenance.
- NP674706.RAlZ5xFxABtnNhXbOa4RjeXmPGWeiWGnsEq2rNo4NtJzg130_assertion evidence source_evidence_literature NP674706.RAlZ5xFxABtnNhXbOa4RjeXmPGWeiWGnsEq2rNo4NtJzg130_provenance.
- NP674706.RAlZ5xFxABtnNhXbOa4RjeXmPGWeiWGnsEq2rNo4NtJzg130_assertion SIO_000772 16679535 NP674706.RAlZ5xFxABtnNhXbOa4RjeXmPGWeiWGnsEq2rNo4NtJzg130_provenance.
- NP674706.RAlZ5xFxABtnNhXbOa4RjeXmPGWeiWGnsEq2rNo4NtJzg130_assertion wasDerivedFrom befree-20150227 NP674706.RAlZ5xFxABtnNhXbOa4RjeXmPGWeiWGnsEq2rNo4NtJzg130_provenance.
- NP674706.RAlZ5xFxABtnNhXbOa4RjeXmPGWeiWGnsEq2rNo4NtJzg130_assertion wasGeneratedBy ECO_0000203 NP674706.RAlZ5xFxABtnNhXbOa4RjeXmPGWeiWGnsEq2rNo4NtJzg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP674706.RAlZ5xFxABtnNhXbOa4RjeXmPGWeiWGnsEq2rNo4NtJzg130_provenance.