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- source_evidence_literature type ECO_0000212 NP404328.RAJhkukKFxggGjnUkM2dIyzoW3s6jf5tbvvuqH-KZlKng130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP404328.RAJhkukKFxggGjnUkM2dIyzoW3s6jf5tbvvuqH-KZlKng130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP404328.RAJhkukKFxggGjnUkM2dIyzoW3s6jf5tbvvuqH-KZlKng130_provenance.
- NP404328.RAJhkukKFxggGjnUkM2dIyzoW3s6jf5tbvvuqH-KZlKng130_assertion description "[The progressive parting of CDKL5- and FOXG1-gene-related encephalopathies from the core Rett syndrome is reflected by the effort to produce clearer diagnostic criteria for typical and atypical Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404328.RAJhkukKFxggGjnUkM2dIyzoW3s6jf5tbvvuqH-KZlKng130_provenance.
- NP404328.RAJhkukKFxggGjnUkM2dIyzoW3s6jf5tbvvuqH-KZlKng130_assertion evidence source_evidence_literature NP404328.RAJhkukKFxggGjnUkM2dIyzoW3s6jf5tbvvuqH-KZlKng130_provenance.
- NP404328.RAJhkukKFxggGjnUkM2dIyzoW3s6jf5tbvvuqH-KZlKng130_assertion SIO_000772 22998673 NP404328.RAJhkukKFxggGjnUkM2dIyzoW3s6jf5tbvvuqH-KZlKng130_provenance.
- NP404328.RAJhkukKFxggGjnUkM2dIyzoW3s6jf5tbvvuqH-KZlKng130_assertion wasDerivedFrom befree-20150227 NP404328.RAJhkukKFxggGjnUkM2dIyzoW3s6jf5tbvvuqH-KZlKng130_provenance.
- NP404328.RAJhkukKFxggGjnUkM2dIyzoW3s6jf5tbvvuqH-KZlKng130_assertion wasGeneratedBy ECO_0000203 NP404328.RAJhkukKFxggGjnUkM2dIyzoW3s6jf5tbvvuqH-KZlKng130_provenance.
- befree-20150227 importedOn "2015-02-27" NP404328.RAJhkukKFxggGjnUkM2dIyzoW3s6jf5tbvvuqH-KZlKng130_provenance.