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- source_evidence_literature type ECO_0000212 NP1048301.RAUDLJ_o6fkkXm6kn5_bSq5giveqLwbeR07Kp37rgju5I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1048301.RAUDLJ_o6fkkXm6kn5_bSq5giveqLwbeR07Kp37rgju5I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1048301.RAUDLJ_o6fkkXm6kn5_bSq5giveqLwbeR07Kp37rgju5I130_provenance.
- NP1048301.RAUDLJ_o6fkkXm6kn5_bSq5giveqLwbeR07Kp37rgju5I130_assertion description "[In this study, we sequenced the TUBB2B and TUBA1A coding regions in 47 patients with a diagnosis of polymicrogyria and five with an atypical lissencephaly on neuroimaging.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1048301.RAUDLJ_o6fkkXm6kn5_bSq5giveqLwbeR07Kp37rgju5I130_provenance.
- NP1048301.RAUDLJ_o6fkkXm6kn5_bSq5giveqLwbeR07Kp37rgju5I130_assertion evidence source_evidence_literature NP1048301.RAUDLJ_o6fkkXm6kn5_bSq5giveqLwbeR07Kp37rgju5I130_provenance.
- NP1048301.RAUDLJ_o6fkkXm6kn5_bSq5giveqLwbeR07Kp37rgju5I130_assertion SIO_000772 23361065 NP1048301.RAUDLJ_o6fkkXm6kn5_bSq5giveqLwbeR07Kp37rgju5I130_provenance.
- NP1048301.RAUDLJ_o6fkkXm6kn5_bSq5giveqLwbeR07Kp37rgju5I130_assertion wasDerivedFrom befree-2016 NP1048301.RAUDLJ_o6fkkXm6kn5_bSq5giveqLwbeR07Kp37rgju5I130_provenance.
- NP1048301.RAUDLJ_o6fkkXm6kn5_bSq5giveqLwbeR07Kp37rgju5I130_assertion wasGeneratedBy ECO_0000203 NP1048301.RAUDLJ_o6fkkXm6kn5_bSq5giveqLwbeR07Kp37rgju5I130_provenance.
- befree-2016 importedOn "2016-02-19" NP1048301.RAUDLJ_o6fkkXm6kn5_bSq5giveqLwbeR07Kp37rgju5I130_provenance.