Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP852966.RAxkJcF6HRm-w5aRT5jLw87H-Uo7lfQkNNx3TZ4TTp25M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP852966.RAxkJcF6HRm-w5aRT5jLw87H-Uo7lfQkNNx3TZ4TTp25M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP852966.RAxkJcF6HRm-w5aRT5jLw87H-Uo7lfQkNNx3TZ4TTp25M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP852966.RAxkJcF6HRm-w5aRT5jLw87H-Uo7lfQkNNx3TZ4TTp25M130_provenance.
- NP852966.RAxkJcF6HRm-w5aRT5jLw87H-Uo7lfQkNNx3TZ4TTp25M130_assertion description "[These genetic changes include haploinsufficiency of SETBP1 associated with intellectual disability and loss of expressive language and truncations of ZMYND11 in individuals with autism, aggression and complex neuropsychiatric features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP852966.RAxkJcF6HRm-w5aRT5jLw87H-Uo7lfQkNNx3TZ4TTp25M130_provenance.
- NP852966.RAxkJcF6HRm-w5aRT5jLw87H-Uo7lfQkNNx3TZ4TTp25M130_assertion evidence source_evidence_literature NP852966.RAxkJcF6HRm-w5aRT5jLw87H-Uo7lfQkNNx3TZ4TTp25M130_provenance.
- NP852966.RAxkJcF6HRm-w5aRT5jLw87H-Uo7lfQkNNx3TZ4TTp25M130_assertion SIO_000772 25217958 NP852966.RAxkJcF6HRm-w5aRT5jLw87H-Uo7lfQkNNx3TZ4TTp25M130_provenance.
- NP852966.RAxkJcF6HRm-w5aRT5jLw87H-Uo7lfQkNNx3TZ4TTp25M130_assertion wasDerivedFrom befree-20150227 NP852966.RAxkJcF6HRm-w5aRT5jLw87H-Uo7lfQkNNx3TZ4TTp25M130_provenance.
- NP852966.RAxkJcF6HRm-w5aRT5jLw87H-Uo7lfQkNNx3TZ4TTp25M130_assertion wasGeneratedBy ECO_0000203 NP852966.RAxkJcF6HRm-w5aRT5jLw87H-Uo7lfQkNNx3TZ4TTp25M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP852966.RAxkJcF6HRm-w5aRT5jLw87H-Uo7lfQkNNx3TZ4TTp25M130_provenance.