Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP901978.RAe8ASf783g-wJSpO384ygHFh4t2nXgwuartXpzjTeog4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP901978.RAe8ASf783g-wJSpO384ygHFh4t2nXgwuartXpzjTeog4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP901978.RAe8ASf783g-wJSpO384ygHFh4t2nXgwuartXpzjTeog4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP901978.RAe8ASf783g-wJSpO384ygHFh4t2nXgwuartXpzjTeog4130_provenance.
- NP901978.RAe8ASf783g-wJSpO384ygHFh4t2nXgwuartXpzjTeog4130_assertion description "[The loss of Cecr2, which encodes a chromatin remodeling protein, has been associated with the neural tube defect (NTD) exencephaly and open eyelids in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP901978.RAe8ASf783g-wJSpO384ygHFh4t2nXgwuartXpzjTeog4130_provenance.
- NP901978.RAe8ASf783g-wJSpO384ygHFh4t2nXgwuartXpzjTeog4130_assertion evidence source_evidence_literature NP901978.RAe8ASf783g-wJSpO384ygHFh4t2nXgwuartXpzjTeog4130_provenance.
- NP901978.RAe8ASf783g-wJSpO384ygHFh4t2nXgwuartXpzjTeog4130_assertion SIO_000772 21246654 NP901978.RAe8ASf783g-wJSpO384ygHFh4t2nXgwuartXpzjTeog4130_provenance.
- NP901978.RAe8ASf783g-wJSpO384ygHFh4t2nXgwuartXpzjTeog4130_assertion wasDerivedFrom befree-20140225 NP901978.RAe8ASf783g-wJSpO384ygHFh4t2nXgwuartXpzjTeog4130_provenance.
- NP901978.RAe8ASf783g-wJSpO384ygHFh4t2nXgwuartXpzjTeog4130_assertion wasGeneratedBy ECO_0000203 NP901978.RAe8ASf783g-wJSpO384ygHFh4t2nXgwuartXpzjTeog4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP901978.RAe8ASf783g-wJSpO384ygHFh4t2nXgwuartXpzjTeog4130_provenance.