Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP850302.RAyHH5o4Qhzc5lLQUkCZrJdAlq6LJU4ypd1b-B_BaxjjY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP850302.RAyHH5o4Qhzc5lLQUkCZrJdAlq6LJU4ypd1b-B_BaxjjY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP850302.RAyHH5o4Qhzc5lLQUkCZrJdAlq6LJU4ypd1b-B_BaxjjY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP850302.RAyHH5o4Qhzc5lLQUkCZrJdAlq6LJU4ypd1b-B_BaxjjY130_provenance.
- NP850302.RAyHH5o4Qhzc5lLQUkCZrJdAlq6LJU4ypd1b-B_BaxjjY130_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." NP850302.RAyHH5o4Qhzc5lLQUkCZrJdAlq6LJU4ypd1b-B_BaxjjY130_provenance.
- NP850302.RAyHH5o4Qhzc5lLQUkCZrJdAlq6LJU4ypd1b-B_BaxjjY130_assertion evidence source_evidence_literature NP850302.RAyHH5o4Qhzc5lLQUkCZrJdAlq6LJU4ypd1b-B_BaxjjY130_provenance.
- NP850302.RAyHH5o4Qhzc5lLQUkCZrJdAlq6LJU4ypd1b-B_BaxjjY130_assertion SIO_000772 11106354 NP850302.RAyHH5o4Qhzc5lLQUkCZrJdAlq6LJU4ypd1b-B_BaxjjY130_provenance.
- NP850302.RAyHH5o4Qhzc5lLQUkCZrJdAlq6LJU4ypd1b-B_BaxjjY130_assertion wasDerivedFrom befree-20150227 NP850302.RAyHH5o4Qhzc5lLQUkCZrJdAlq6LJU4ypd1b-B_BaxjjY130_provenance.
- NP850302.RAyHH5o4Qhzc5lLQUkCZrJdAlq6LJU4ypd1b-B_BaxjjY130_assertion wasGeneratedBy ECO_0000203 NP850302.RAyHH5o4Qhzc5lLQUkCZrJdAlq6LJU4ypd1b-B_BaxjjY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP850302.RAyHH5o4Qhzc5lLQUkCZrJdAlq6LJU4ypd1b-B_BaxjjY130_provenance.