Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1064761.RAIsMWSx7XOYrTN1JnIDwQitEx0P5KD-Af0if7KD1ShB4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1064761.RAIsMWSx7XOYrTN1JnIDwQitEx0P5KD-Af0if7KD1ShB4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1064761.RAIsMWSx7XOYrTN1JnIDwQitEx0P5KD-Af0if7KD1ShB4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1064761.RAIsMWSx7XOYrTN1JnIDwQitEx0P5KD-Af0if7KD1ShB4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1064761.RAIsMWSx7XOYrTN1JnIDwQitEx0P5KD-Af0if7KD1ShB4130_provenance.
- NP1064761.RAIsMWSx7XOYrTN1JnIDwQitEx0P5KD-Af0if7KD1ShB4130_assertion wasGeneratedBy ECO_0000203 NP1064761.RAIsMWSx7XOYrTN1JnIDwQitEx0P5KD-Af0if7KD1ShB4130_provenance.
- NP1064761.RAIsMWSx7XOYrTN1JnIDwQitEx0P5KD-Af0if7KD1ShB4130_assertion wasDerivedFrom befree-2016 NP1064761.RAIsMWSx7XOYrTN1JnIDwQitEx0P5KD-Af0if7KD1ShB4130_provenance.
- NP1064761.RAIsMWSx7XOYrTN1JnIDwQitEx0P5KD-Af0if7KD1ShB4130_assertion SIO_000772 23539225 NP1064761.RAIsMWSx7XOYrTN1JnIDwQitEx0P5KD-Af0if7KD1ShB4130_provenance.
- NP1064761.RAIsMWSx7XOYrTN1JnIDwQitEx0P5KD-Af0if7KD1ShB4130_assertion evidence source_evidence_literature NP1064761.RAIsMWSx7XOYrTN1JnIDwQitEx0P5KD-Af0if7KD1ShB4130_provenance.
- NP1064761.RAIsMWSx7XOYrTN1JnIDwQitEx0P5KD-Af0if7KD1ShB4130_assertion description "[Severe prenatal renal anomalies associated with mutations in HNF1B or PAX2 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1064761.RAIsMWSx7XOYrTN1JnIDwQitEx0P5KD-Af0if7KD1ShB4130_provenance.