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- source_evidence_literature type ECO_0000212 NP302229.RAyC_hbLY8tCk7MXW3f5QbBNGrbQoFyWoHIa6OI74tXaQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP302229.RAyC_hbLY8tCk7MXW3f5QbBNGrbQoFyWoHIa6OI74tXaQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP302229.RAyC_hbLY8tCk7MXW3f5QbBNGrbQoFyWoHIa6OI74tXaQ130_provenance.
- NP302229.RAyC_hbLY8tCk7MXW3f5QbBNGrbQoFyWoHIa6OI74tXaQ130_assertion description "[The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP302229.RAyC_hbLY8tCk7MXW3f5QbBNGrbQoFyWoHIa6OI74tXaQ130_provenance.
- NP302229.RAyC_hbLY8tCk7MXW3f5QbBNGrbQoFyWoHIa6OI74tXaQ130_assertion evidence source_evidence_literature NP302229.RAyC_hbLY8tCk7MXW3f5QbBNGrbQoFyWoHIa6OI74tXaQ130_provenance.
- NP302229.RAyC_hbLY8tCk7MXW3f5QbBNGrbQoFyWoHIa6OI74tXaQ130_assertion SIO_000772 11106354 NP302229.RAyC_hbLY8tCk7MXW3f5QbBNGrbQoFyWoHIa6OI74tXaQ130_provenance.
- NP302229.RAyC_hbLY8tCk7MXW3f5QbBNGrbQoFyWoHIa6OI74tXaQ130_assertion wasDerivedFrom befree-2016 NP302229.RAyC_hbLY8tCk7MXW3f5QbBNGrbQoFyWoHIa6OI74tXaQ130_provenance.
- NP302229.RAyC_hbLY8tCk7MXW3f5QbBNGrbQoFyWoHIa6OI74tXaQ130_assertion wasGeneratedBy ECO_0000203 NP302229.RAyC_hbLY8tCk7MXW3f5QbBNGrbQoFyWoHIa6OI74tXaQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP302229.RAyC_hbLY8tCk7MXW3f5QbBNGrbQoFyWoHIa6OI74tXaQ130_provenance.