Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1064761.RAIsMWSx7XOYrTN1JnIDwQitEx0P5KD-Af0if7KD1ShB4130_assertion> ?p ?o ?g. }
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- NP1064761.RAIsMWSx7XOYrTN1JnIDwQitEx0P5KD-Af0if7KD1ShB4130_assertion type Assertion NP1064761.RAIsMWSx7XOYrTN1JnIDwQitEx0P5KD-Af0if7KD1ShB4130_head.
- 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.