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- source_evidence_literature type ECO_0000212 NP651456.RALJldoHwb7pxF5VmVPYd7PP9aBtdRZFQz-Ahl7z_j2X0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP651456.RALJldoHwb7pxF5VmVPYd7PP9aBtdRZFQz-Ahl7z_j2X0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP651456.RALJldoHwb7pxF5VmVPYd7PP9aBtdRZFQz-Ahl7z_j2X0130_provenance.
- NP651456.RALJldoHwb7pxF5VmVPYd7PP9aBtdRZFQz-Ahl7z_j2X0130_assertion description "[We recently identified the four and a half LIM domain gene FHL1 located on chromosome Xq26 as the causative gene for RBM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651456.RALJldoHwb7pxF5VmVPYd7PP9aBtdRZFQz-Ahl7z_j2X0130_provenance.
- NP651456.RALJldoHwb7pxF5VmVPYd7PP9aBtdRZFQz-Ahl7z_j2X0130_assertion evidence source_evidence_literature NP651456.RALJldoHwb7pxF5VmVPYd7PP9aBtdRZFQz-Ahl7z_j2X0130_provenance.
- NP651456.RALJldoHwb7pxF5VmVPYd7PP9aBtdRZFQz-Ahl7z_j2X0130_assertion SIO_000772 20571991 NP651456.RALJldoHwb7pxF5VmVPYd7PP9aBtdRZFQz-Ahl7z_j2X0130_provenance.
- NP651456.RALJldoHwb7pxF5VmVPYd7PP9aBtdRZFQz-Ahl7z_j2X0130_assertion wasDerivedFrom befree-20140225 NP651456.RALJldoHwb7pxF5VmVPYd7PP9aBtdRZFQz-Ahl7z_j2X0130_provenance.
- NP651456.RALJldoHwb7pxF5VmVPYd7PP9aBtdRZFQz-Ahl7z_j2X0130_assertion wasGeneratedBy ECO_0000203 NP651456.RALJldoHwb7pxF5VmVPYd7PP9aBtdRZFQz-Ahl7z_j2X0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP651456.RALJldoHwb7pxF5VmVPYd7PP9aBtdRZFQz-Ahl7z_j2X0130_provenance.