Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP560986.RAPzxJJbLrybEFYATODM9HqiR4ZHz40U-KXpPLES0zfOU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP560986.RAPzxJJbLrybEFYATODM9HqiR4ZHz40U-KXpPLES0zfOU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP560986.RAPzxJJbLrybEFYATODM9HqiR4ZHz40U-KXpPLES0zfOU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP560986.RAPzxJJbLrybEFYATODM9HqiR4ZHz40U-KXpPLES0zfOU130_provenance.
- NP560986.RAPzxJJbLrybEFYATODM9HqiR4ZHz40U-KXpPLES0zfOU130_assertion description "[Additionally, the NLGN3 transcript was present in two isoforms (with and without exon 7) in nine of 10 autistic females and in 30 non-autistic subjects, including parents of the autistic female having only the complete transcript with exon 7, and from the whole brain of a control.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP560986.RAPzxJJbLrybEFYATODM9HqiR4ZHz40U-KXpPLES0zfOU130_provenance.
- NP560986.RAPzxJJbLrybEFYATODM9HqiR4ZHz40U-KXpPLES0zfOU130_assertion evidence source_evidence_literature NP560986.RAPzxJJbLrybEFYATODM9HqiR4ZHz40U-KXpPLES0zfOU130_provenance.
- NP560986.RAPzxJJbLrybEFYATODM9HqiR4ZHz40U-KXpPLES0zfOU130_assertion SIO_000772 16648374 NP560986.RAPzxJJbLrybEFYATODM9HqiR4ZHz40U-KXpPLES0zfOU130_provenance.
- NP560986.RAPzxJJbLrybEFYATODM9HqiR4ZHz40U-KXpPLES0zfOU130_assertion wasDerivedFrom befree-20140225 NP560986.RAPzxJJbLrybEFYATODM9HqiR4ZHz40U-KXpPLES0zfOU130_provenance.
- NP560986.RAPzxJJbLrybEFYATODM9HqiR4ZHz40U-KXpPLES0zfOU130_assertion wasGeneratedBy ECO_0000203 NP560986.RAPzxJJbLrybEFYATODM9HqiR4ZHz40U-KXpPLES0zfOU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP560986.RAPzxJJbLrybEFYATODM9HqiR4ZHz40U-KXpPLES0zfOU130_provenance.