Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP385285.RAb2kPn7K3ZpzMA8hkR3uF9jo0aBug2hOitn_Ft2LPQ04130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP385285.RAb2kPn7K3ZpzMA8hkR3uF9jo0aBug2hOitn_Ft2LPQ04130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP385285.RAb2kPn7K3ZpzMA8hkR3uF9jo0aBug2hOitn_Ft2LPQ04130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP385285.RAb2kPn7K3ZpzMA8hkR3uF9jo0aBug2hOitn_Ft2LPQ04130_provenance.
- befree-2016 importedOn "2016-02-19" NP385285.RAb2kPn7K3ZpzMA8hkR3uF9jo0aBug2hOitn_Ft2LPQ04130_provenance.
- NP385285.RAb2kPn7K3ZpzMA8hkR3uF9jo0aBug2hOitn_Ft2LPQ04130_assertion wasGeneratedBy ECO_0000203 NP385285.RAb2kPn7K3ZpzMA8hkR3uF9jo0aBug2hOitn_Ft2LPQ04130_provenance.
- NP385285.RAb2kPn7K3ZpzMA8hkR3uF9jo0aBug2hOitn_Ft2LPQ04130_assertion wasDerivedFrom befree-2016 NP385285.RAb2kPn7K3ZpzMA8hkR3uF9jo0aBug2hOitn_Ft2LPQ04130_provenance.
- NP385285.RAb2kPn7K3ZpzMA8hkR3uF9jo0aBug2hOitn_Ft2LPQ04130_assertion SIO_000772 12610651 NP385285.RAb2kPn7K3ZpzMA8hkR3uF9jo0aBug2hOitn_Ft2LPQ04130_provenance.
- NP385285.RAb2kPn7K3ZpzMA8hkR3uF9jo0aBug2hOitn_Ft2LPQ04130_assertion evidence source_evidence_literature NP385285.RAb2kPn7K3ZpzMA8hkR3uF9jo0aBug2hOitn_Ft2LPQ04130_provenance.
- NP385285.RAb2kPn7K3ZpzMA8hkR3uF9jo0aBug2hOitn_Ft2LPQ04130_assertion description "[R542Q in SCN1A was observed in one autism family and had previously been identified in a patient with juvenile myoclonic epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP385285.RAb2kPn7K3ZpzMA8hkR3uF9jo0aBug2hOitn_Ft2LPQ04130_provenance.