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- source_evidence_literature type ECO_0000212 NP1008015.RANI2cQqQe60B6ToFeTj0vn1DIVb-XZxt4jWxH2Wmz9Zo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1008015.RANI2cQqQe60B6ToFeTj0vn1DIVb-XZxt4jWxH2Wmz9Zo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1008015.RANI2cQqQe60B6ToFeTj0vn1DIVb-XZxt4jWxH2Wmz9Zo130_provenance.
- NP1008015.RANI2cQqQe60B6ToFeTj0vn1DIVb-XZxt4jWxH2Wmz9Zo130_assertion description "[The authors report detailed clinical and developmental assessment of 3 brothers who were found to carry a novel mutation in the ARX gene associated with a relatively mild phenotype of static global developmental delay and early hand preference.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1008015.RANI2cQqQe60B6ToFeTj0vn1DIVb-XZxt4jWxH2Wmz9Zo130_provenance.
- NP1008015.RANI2cQqQe60B6ToFeTj0vn1DIVb-XZxt4jWxH2Wmz9Zo130_assertion evidence source_evidence_literature NP1008015.RANI2cQqQe60B6ToFeTj0vn1DIVb-XZxt4jWxH2Wmz9Zo130_provenance.
- NP1008015.RANI2cQqQe60B6ToFeTj0vn1DIVb-XZxt4jWxH2Wmz9Zo130_assertion SIO_000772 22922607 NP1008015.RANI2cQqQe60B6ToFeTj0vn1DIVb-XZxt4jWxH2Wmz9Zo130_provenance.
- NP1008015.RANI2cQqQe60B6ToFeTj0vn1DIVb-XZxt4jWxH2Wmz9Zo130_assertion wasDerivedFrom befree-2016 NP1008015.RANI2cQqQe60B6ToFeTj0vn1DIVb-XZxt4jWxH2Wmz9Zo130_provenance.
- NP1008015.RANI2cQqQe60B6ToFeTj0vn1DIVb-XZxt4jWxH2Wmz9Zo130_assertion wasGeneratedBy ECO_0000203 NP1008015.RANI2cQqQe60B6ToFeTj0vn1DIVb-XZxt4jWxH2Wmz9Zo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1008015.RANI2cQqQe60B6ToFeTj0vn1DIVb-XZxt4jWxH2Wmz9Zo130_provenance.