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- source_evidence_literature type ECO_0000212 NP978189.RAwAcL-ZhIsKhgzbHw4Ad9v4IW7UljDHnh189o6c-zi1g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978189.RAwAcL-ZhIsKhgzbHw4Ad9v4IW7UljDHnh189o6c-zi1g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978189.RAwAcL-ZhIsKhgzbHw4Ad9v4IW7UljDHnh189o6c-zi1g130_provenance.
- NP978189.RAwAcL-ZhIsKhgzbHw4Ad9v4IW7UljDHnh189o6c-zi1g130_assertion description "[Mutations in the Aristaless-related homeobox gene, ARX, have been a cause of X-linked mental retardation (XLMR) and are responsible for a vast phenotypic spectrum including syndromic and non-syndromic forms of mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978189.RAwAcL-ZhIsKhgzbHw4Ad9v4IW7UljDHnh189o6c-zi1g130_provenance.
- NP978189.RAwAcL-ZhIsKhgzbHw4Ad9v4IW7UljDHnh189o6c-zi1g130_assertion evidence source_evidence_literature NP978189.RAwAcL-ZhIsKhgzbHw4Ad9v4IW7UljDHnh189o6c-zi1g130_provenance.
- NP978189.RAwAcL-ZhIsKhgzbHw4Ad9v4IW7UljDHnh189o6c-zi1g130_assertion SIO_000772 17613295 NP978189.RAwAcL-ZhIsKhgzbHw4Ad9v4IW7UljDHnh189o6c-zi1g130_provenance.
- NP978189.RAwAcL-ZhIsKhgzbHw4Ad9v4IW7UljDHnh189o6c-zi1g130_assertion wasDerivedFrom befree-20150227 NP978189.RAwAcL-ZhIsKhgzbHw4Ad9v4IW7UljDHnh189o6c-zi1g130_provenance.
- NP978189.RAwAcL-ZhIsKhgzbHw4Ad9v4IW7UljDHnh189o6c-zi1g130_assertion wasGeneratedBy ECO_0000203 NP978189.RAwAcL-ZhIsKhgzbHw4Ad9v4IW7UljDHnh189o6c-zi1g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978189.RAwAcL-ZhIsKhgzbHw4Ad9v4IW7UljDHnh189o6c-zi1g130_provenance.