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- source_evidence_literature type ECO_0000212 NP518630.RA4LwB-J8bBMpnZOM1kytjgmYPypVmrkwIaguRVftgLE0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP518630.RA4LwB-J8bBMpnZOM1kytjgmYPypVmrkwIaguRVftgLE0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP518630.RA4LwB-J8bBMpnZOM1kytjgmYPypVmrkwIaguRVftgLE0130_provenance.
- NP518630.RA4LwB-J8bBMpnZOM1kytjgmYPypVmrkwIaguRVftgLE0130_assertion description "[Mutations in the human ARX gene have been shown to cause nonsyndromic X-linked mental retardation (MRX) as well as syndromic forms such as X-linked lissencephaly with abnormal genitalia (XLAG), Partington syndrome and X-linked infantile spasm.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP518630.RA4LwB-J8bBMpnZOM1kytjgmYPypVmrkwIaguRVftgLE0130_provenance.
- NP518630.RA4LwB-J8bBMpnZOM1kytjgmYPypVmrkwIaguRVftgLE0130_assertion evidence source_evidence_literature NP518630.RA4LwB-J8bBMpnZOM1kytjgmYPypVmrkwIaguRVftgLE0130_provenance.
- NP518630.RA4LwB-J8bBMpnZOM1kytjgmYPypVmrkwIaguRVftgLE0130_assertion SIO_000772 16235064 NP518630.RA4LwB-J8bBMpnZOM1kytjgmYPypVmrkwIaguRVftgLE0130_provenance.
- NP518630.RA4LwB-J8bBMpnZOM1kytjgmYPypVmrkwIaguRVftgLE0130_assertion wasDerivedFrom befree-2016 NP518630.RA4LwB-J8bBMpnZOM1kytjgmYPypVmrkwIaguRVftgLE0130_provenance.
- NP518630.RA4LwB-J8bBMpnZOM1kytjgmYPypVmrkwIaguRVftgLE0130_assertion wasGeneratedBy ECO_0000203 NP518630.RA4LwB-J8bBMpnZOM1kytjgmYPypVmrkwIaguRVftgLE0130_provenance.
- befree-2016 importedOn "2016-02-19" NP518630.RA4LwB-J8bBMpnZOM1kytjgmYPypVmrkwIaguRVftgLE0130_provenance.