Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1168960.RAcN2g1X1hyJksy5W1d1sB4LwRi9acH9CZ431qBc1iKro130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1168960.RAcN2g1X1hyJksy5W1d1sB4LwRi9acH9CZ431qBc1iKro130_assertion type Assertion NP1168960.RAcN2g1X1hyJksy5W1d1sB4LwRi9acH9CZ431qBc1iKro130_head.
- NP1168960.RAcN2g1X1hyJksy5W1d1sB4LwRi9acH9CZ431qBc1iKro130_assertion description "[Mutations in CFTR are responsible for cystic fibrosis, CF, an autosomal recessive disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1168960.RAcN2g1X1hyJksy5W1d1sB4LwRi9acH9CZ431qBc1iKro130_provenance.
- NP1168960.RAcN2g1X1hyJksy5W1d1sB4LwRi9acH9CZ431qBc1iKro130_assertion evidence source_evidence_literature NP1168960.RAcN2g1X1hyJksy5W1d1sB4LwRi9acH9CZ431qBc1iKro130_provenance.
- NP1168960.RAcN2g1X1hyJksy5W1d1sB4LwRi9acH9CZ431qBc1iKro130_assertion SIO_000772 24685681 NP1168960.RAcN2g1X1hyJksy5W1d1sB4LwRi9acH9CZ431qBc1iKro130_provenance.
- NP1168960.RAcN2g1X1hyJksy5W1d1sB4LwRi9acH9CZ431qBc1iKro130_assertion wasDerivedFrom befree-2016 NP1168960.RAcN2g1X1hyJksy5W1d1sB4LwRi9acH9CZ431qBc1iKro130_provenance.
- NP1168960.RAcN2g1X1hyJksy5W1d1sB4LwRi9acH9CZ431qBc1iKro130_assertion wasGeneratedBy ECO_0000203 NP1168960.RAcN2g1X1hyJksy5W1d1sB4LwRi9acH9CZ431qBc1iKro130_provenance.